LUNA MEDICAL TECHNOLOGIES INC
10SB12B/A, 1999-11-23
IN VITRO & IN VIVO DIAGNOSTIC SUBSTANCES
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                     U.S. SECURITIES AND EXCHANGE COMMISSION
                             Washington, D.C. 20549

                               AMENDMENT NO. 2 TO
                                   FORM 10-SB

                   GENERAL FORM FOR REGISTRATION OF SECURITIES
                            OF SMALL BUSINESS ISSUERS

                         Under Section 12(b) or 12(g) of
                       The Securities Exchange Act of 1934

                        LUNA MEDICAL TECHNOLOGIES, INC.,
                              a Nevada corporation
             (Exact name of registrant as specified in its charter)

NEVADA                                                                98-0207745
- ------                                                                ----------
(State or other jurisdiction of             (I.R.S. Employer Identification No.)
incorporation or organization)

1820-1095 West Pender Street, Vancouver, British Columbia, Canada        V6E 2M6
- --------------------------------------------------------------------------------
(Address of registrant's principal executive offices)                 (Zip Code)

                                  604.687.0719
                                  ------------
              (Registrant's Telephone Number, Including Area Code)

Securities to be registered under Section 12(b) of the Act:

          Title of Each Class               Name of Each Exchange on which
          to be so Registered:              Each Class is to be Registered:
          --------------------              -------------------------------

                 None                                   None
                 ----                                   ----

Securities to be registered under Section 12(g) of the Act:

    Common Stock, Par Value $.001          Preferred Stock, Par Value $.001
    -----------------------------          --------------------------------
           (Title of Class)                        (Title of Class)

                                   Copies to:

                              Thomas E. Stepp, Jr.
                             Stepp & Beauchamp, LLP
                           1301 Dove Street, Suite 460
                         Newport Beach, California 92660
                                  949.660.9700
                             Facsimile: 949.660.9010

                                  Page 1 of 12
                      Exhibit Index is specified on Page 11

<PAGE>

                         Luna Medical Technologies, Inc.
                              a Nevada corporation

          Index to Amendment No. 2 to Form 10-SB Registration Statement

Item Number and Caption                                                    Page
- -----------------------                                                    ----

1.    Description of Business................................................3
          Development of the Company.........................................3
          Business of the Company............................................3
          Government Approval................................................4
          Patents............................................................4
          The Company's Subsidiary ..........................................5
          Marketing and Sales Strategy.......................................5
          Competition........................................................6
          Personal Fertility Technologies, Inc. ("PFT")......................6
          Med-Direct Products Inc. ("MDP")...................................6
          Natural Family Planning Using the Luna Fertility Indicator.........7
          Basic Fertility Awareness..........................................7
          Other Methods of Natural Family Planning...........................7
          Employees..........................................................7
          Reports to Security Holders........................................8
2.    Management's Discussion and Analysis of Financial Condition and
          Results of Operations..............................................8
          Revenue............................................................8
          Costs and Expenses.................................................8
          Liquidity and Capital Resources....................................8
          Results of Operations.............................................10
          Year 2000 Compliance..............................................10
3.    Description of Property...............................................10
      Property Held by the Company .........................................10
11.   Description of Securities.............................................10
15b.  Exhibits..............................................................11

Signatures    ..............................................................12


                                       2
<PAGE>

Item 1. Description of Business.

Development  of  the  Company.  Luna  Medical   Technologies,   Inc.,  a  Nevada
corporation  ("Company"),   formerly  entitled  Luna  Technologies,   Inc.,  was
incorporated  in the State of Nevada on January  19,  1999.  On or about May 31,
1999,  the  Company  changed its name to Luna  Medical  Technologies,  Inc.  The
executive  offices of the Company are located at 1820-1095  West Pender  Street,
Vancouver,  British Columbia,  Canada V6E 2M6. The Company's telephone number is
604.687.0719.

Business of the Company.  On or about January 31, 1999, the Company entered into
an exclusive worldwide license agreement ("Agreement") with Luna Products, Inc.,
a Canadian  corporation  ("LPI"),  to distribute  the Luna  Fertility  Indicator
("Indicator"),  a  lightweight,  re-usable  home  fertility  test. As a point of
clarification,  as used in this  Amendment No. 2 to the  Company's  Registration
Statement  on Form 10-SB the term "US$" means and refers to the  currency of the
United States of America, unless otherwise stated. As used in this Amendment No.
2 to the  Company's  Registration  Statement on Form 10-SB the term "CDN$" means
the  currency of Canada,  in Canadian  Dollars,  unless  otherwise  stated.  The
Agreement also grants the Company the right to distribute  fertility charts with
every purchase of the Indicator  (described in more detail  below).  In exchange
for the grant of the worldwide license  ("License"),  the Company agreed to lend
LPI  US$40,000,  interest  free  ("Loan"),  and spend a minimum of  US$20,000 on
marketing the Indicator. The Agreement provides that LPI shall repay the Loan by
paying to the Company a fee of CDN$1.00  for each  Indicator  sold for the first
30,000  Indicators  sold, then CDN$.50 per Indicator sold in perpetuity.  LPI is
not required to repay the Loan within any specified  period of time. The term of
the Loan will be dependent on the number of Indicators sold by the Company.  The
Company  was also  given  the  option  of  converting  the Loan to a 50%  equity
interest in LPI, in which case LPI would have no obligation to repay the Loan or
any  royalties.  The  Company  also  agreed to pay LPI a 5% royalty on the total
gross  sales of the  Indicator  during the term of the  License.  Moreover,  the
Company agreed to pay directly to Jim Emmerson,  a director of LPI, a royalty of
CDN$1.00  per  Indicator  sold in  perpetuity.  The  license  granted  under the
Agreement expires upon repayment of the Loan. However,  the Company and LPI have
orally  agreed that the  relationship  between the Company and LPI will continue
beyond the term of the License.  The Company anticipates that the specific terms
and conditions of any continuing  relationship will be substantially  similar to
those  contained  in the  Agreement.  However,  the Company and LPI have not yet
finalized the specific  terms and conditions of their  continuing  relationship.
Except for their relationship regarding the Indicator,  the Company and LPI have
no other affiliation.

On or about May 6,  1999,  the  Company  and LPI  agreed to amend the  Agreement
("Amendment").  Among other things, the Company agreed not to exercise its right
to  convert  the Loan to a 50%  equity  interest  in LPI.  LPI  agreed  that the
Indicator  would be sold to the Company for  CDN$12.50,  if the Company sold the
Indicator to wholesalers and distributors, and CDN$16.50 if the Company sold the
Indicator   directly  to   consumers.   The  Company  also  agreed  to  increase
expenditures  for marketing the Indicator to CDN$250,000 or more, to be expended
on or before May 31, 2000. The exclusive  marketing  rights and royalty payments
provided for under the Agreement and those terms and conditions contained in the
Amendment,  apply to the Indicator and any modified version of the Indicator but
do not apply to other products that may be developed by LPI.

The concept behind the Indicator has been used in Europe for some time. Although
no product  exactly  like the  Indicator  is being sold in Europe,  the  Company
believes that the medical principles behind the Indicator involving the analysis
of a woman's  saliva to  determine  fertility  have been the subject of clinical
tests to verify  the  safety  of that  concept.  However,  the  Company  has not
conducted  its own testing  regarding  the accuracy of the  Indicator and cannot
attest to the extent,  nature,  accuracy  or validity of any third party  tests.
Quite  simply,  a woman's body fluids  indicate  the changes in hormones  during
different  phases of her  fertility  cycle.  When the dried  fluids  are  viewed
through a powerful  magnifier,  patterns in the crystallized fluids indicate the
stage of her  fertility  cycle.  The  Indicator  relies on the medical fact that
saliva  crystallizes in the same special way as uterine  cervical mucus,  due to
the action of the estrogens, presenting the appearance of fern-type branches. In
1948, Dr. Ridborg first discovered  physiological variations in the crystallized
arrangement of saliva (or cervical  uterine mucus) related to ovulation.  Later,
Doctors Evelyn L. and John J. Billings  identified this scientific  discovery as
an indicator of female  fertility.


                                       3
<PAGE>

The Company cannot attest to the accuracy,  extent,  nature or validity of those
tests conducted by Evelyn and John Billings.

In 1969,  at the Royal  Academy  of  Medicine  in  Barcelona,  Spain,  Dr.  Biel
documented his  investigations  evidencing  the  relationship  between  hormonal
changes during the menstrual cycle and  crystallization  of female saliva during
ovulation,  which  followed  an  identical  pattern in uterine  cervical  mucus.
Specifically,  a woman's  saliva and  uterine  cervical  mucus only  crystallize
during a period of from 6 to 8 days,  during the fertile  stage of the menstrual
and ovulation cycle. It is important to note that individual advances and delays
in  ovulation do not affect this  method's  precision,  as the method  relies on
ovulation  itself rather than a projected  cycle date. The Company cannot attest
to the  accuracy,  extent,  nature or validity of those tests  conducted  by Dr.
Biel.

The  secretion  of estrogen  and  progesterone  changes  daily  during a woman's
menstrual cycle,  influencing the characteristics,  which can be observed in the
dried body fluids,  in particular,  saliva and cervical fluid.  These observable
characteristics include an increase in filaceousness (that is, the appearance of
thread-type  anatomical  structures)  and  specific  changes in the  crystalline
patterns  during the days preceding  ovulation.  The increase of estrogen during
the whole of the first  stage of the  menstrual  cycle  produces  changes in the
consistency  and  crystallization  of  saliva,  in the  same  way as in  uterine
cervical mucus. The estrogens only produce  crystallization of these fluids when
they reach a certain  concentration.  This  concentration is reached 3 to 4 days
prior to ovulation.

The simple  procedure to produce and examine  these  crystalline  patterns is by
placing a saliva (or cervical  mucus fluid)  sample on a slide to evaporate  and
view  through a small,  powerful,  hand-held  microscope.  By  repeated  in-home
testing,  a woman can track her complete ovulation cycle without the nuisance of
urine tests,  temperature tests and monthly calendar tracking,  or costly visits
to a fertility or health care service. It is totally private,  non-invasive, and
chemical free method of testing for fertility.

The  Indicator  takes up slightly more space than a lipstick and can be used any
private  place with access to natural or clear light.  A woman  simply  places a
sample of her saliva on the clean  slide,  allows the saliva to dry,  then holds
the  slide up to a 40-watt  or  greater  light  source  and looks at the  saliva
pattern  through  the  eyepiece.  The woman then  compares  her saliva  patterns
indicated  in the book of charts  provided  free of charge  with the  Indicator.
Comparing the saliva  patterns will indicate her state of fertility.  The charts
are easy to use,  consisting mainly of the woman noting on the chart whether she
is fertile or infertile based on the saliva patterns, thus providing a quick and
easy reference  indicating her monthly  fertility  cycle. If the woman is in the
biologically  active,  fertile phase,  her saliva will  crystallize  and fibrous
"fern-type" patterns will be clearly viewed in the small Indicator in-home small
microscope. Then she can rinse off the slide and put it away until the next use.

The Company  anticipates that the Indicator will be used as a guide to determine
the  different  phases  of the  fertility  cycle  and  as an  aid  to  encourage
conception. The Company does not intend for this device to be used or considered
as a  contraceptive  or method of birth  control.  The  distinction  lies in the
difference between  anti-procreative sex (contraception) and non-procreative sex
(natural family planning).  Please refer to the section entitled "Natural Family
Planning using the Luna Fertility Indicator" on page 6.

Government  Approval.  In order to sell the  Company's  product in  Canada,  the
Company was required to obtain a Drug Identification Number ("DIN"). The Company
has applied for and received DIN186759.

In order to sell the  Company's  products in the United  States,  the Company is
currently preparing the requisite filing documents for application with the Food
and Drug Administration ("FDA"). The Company expects that the initial FDA filing
will occur  within the next 60 days.  The Company  anticipates  that because the
Indicator is non-invasive,  the FDA application  process will take approximately
six (6) months to  complete.  The  Company  anticipates  that it will market the
Indicator to various countries and will at that time make the proper application
for any  required  governmental  approvals.  At this time,  the  Company has not
applied for any additional governmental approvals.

Patents.  LPI has  applied  for and  received a Canadian  design  patent for the
manufacture  of the  Indicator.  The Company has not been assigned any ownership
rights in that Canadian patent.  Neither LPI nor the Company have


                                       4
<PAGE>

either  applied for or obtained a United States patent  covering the  Indicator.
The Company  regards  certain  aspects of the Indicator as proprietary  and will
attempt to protect such proprietary information through contractual restrictions
on disclosure,  copying and  distribution.  The Company itself does not hold any
patents. Except as protected by the Canadian patent held by LPI, there can be no
assurance  that  the  Company's   competitors  will  not  independently  develop
technologies that are  substantially  equivalent or superior to the Company's or
LPI's technologies.  While the Company believes that its rights in the Indicator
do not and will not  infringe  or violate  proprietary  rights of others,  it is
possible that  infringement of proprietary  rights of others may occur. Any such
claims,  with or without  merit,  can be time  consuming and difficult to defend
and, if successful, could have a material adverse effect on the Company.

The Company's  Subsidiary.  On or about May 11, 1999,  the Company  caused to be
incorporated, in British Columbia, Luna Fertility Indicator, Inc. Luna Fertility
Indicator,  Inc., is currently a  wholly-owned  subsidiary  of the Company.  The
Company anticipates that the primary business of Luna Fertility Indicator, Inc.,
will be marketing and distributing the Indicator.

Marketing  and Sales  Strategy.  The Company has hired,  on an as needed  basis,
Melissa Gervais to act as an in-house marketing and public relations  consultant
to  co-ordinate  an  advertising  campaign  in  targeted  media  such as medical
journals,  women's magazines,  religious  publications and other selected media.
From January 19, 1999  (inception)  through June 30, 1999,  the Company has paid
Ms. Gervais a total of US$16,830 in consulting  fees. The Company hopes that Ms.
Gervais' efforts will help generate  immediate  awareness of the Indicator.  The
Company  will  attempt to market the  Indicator in major chain drug stores using
selected regional distributors.

The Company has agreed in principal on a  distribution  contract  with  Bathurst
Sales  ("Bathurst")  of Downsview,  Ontario,  Canada's  leading  distributor  of
cosmetics and personal care  products,  whose  customers  include  London Drugs,
Shoppers  Drug Mart,  Pharma Plus  Drugmarts,  Lawton's Drug Stores and Uniprix.
Bathurst  distributes  products such as Revlon,  John Frieda,  Elizabeth  Arden,
Rubbermaid,  AM Cosmetics and Vogue  International,  and its current clients are
those that the Company  desires will market and promote the Indicator.  Bathurst
will  be  informed  of  the  dates  of the  Company's  advertising  programs  to
co-ordinate any co-operative advertising plans that its clients may have for the
period.  Bathurst has orally agreed to distribute the Indicator and negotiations
are  ongoing to reduce the terms,  conditions  and  covenants  to  writing.  The
Company  anticipates that the written agreement between the Company and Bathurst
will provide for the shipment, FOB Vancouver, on a CDN$22.00 per unit basis.

The Company is in the process of developing  new and  attractive  ways to market
the  Indicator.  During the last  several  months,  the Company has designed new
packaging and marketing  materials  which the Company  believes will enhance the
appeal of the Indicator. The Indicator is now being represented in Canada by two
distributors.  The  first  distributor,  Bathurst,  sells  various  products  to
traditional  drug  stores.  The second  distributor,  Inno-Vite,  sells  various
products  to  health  food  stores  such as  Caper's,  Vitamin  House,  Choices,
Nutrition  House,  GNC and  Noah's  Natural  Foods.  The  Company  continues  to
negotiate  with the companies  interested  in the  Company's  Indicator in other
markets  throughout  the  world.  The  Company   anticipates  that  distribution
arrangements  will be finalized  within six (6) months of securing the necessary
governmental approvals in those foreign markets.

The Company is also involved in the  advertising  and promotion of the Indicator
on the  Internet.  The  Company's  Internet  website  is  www.lunafert.com.  The
Company's  website contains general  information on (i) how the Indicator works;
(ii) frequently asked questions; (iii) the chart (more particularly described on
page 4, Item 1); (iv) where to purchase the Indicator  (such  information  lists
locations in only those  jurisdictions where the Indicator may be sold); (v) the
Company.  The Company does not  anticipate  that it will engage in e-commerce in
the near future.  However,  should the Company  decide to sell the Indicator via
its website, it plans to take all of the necessary  precautions to ensure secure
transmission of confidential information, including, but not necessarily limited
to, the reliance on encryption and  authentication  technology.  Currently,  the
Company's website is for informational  purposes only. Moreover,  the content is
limited and no products are sold via the Company's website. The


                                       5
<PAGE>

costs associated with developing and maintaining the Company's website have been
minimal.  The Company does not anticipate any material  expenditures  within the
next  12-months  associated  with its  website.  Any costs  associated  with the
Company's  website  will be minimal and the Company  believes it has  sufficient
funds to  maintain  its  website.  The  Company  does not  currently  have  link
arrangements with any other websites nor does it have any tie-ins with any other
websites nor does it have any tie-ins with any search engines.

The Company has  commenced  sales of the  Indicator  in Canada.  The Company has
focused its initial sales efforts in Canada  because it has received  government
approval to  distribute  the  Indicator.  The Company  anticipates  that it will
initiate a mail order  campaign and  advertising in selected  publications.  The
Company has begun discussing with potential distributors in Taiwan, South Africa
and Turkey the potential foreign markets for the Indicator. The Company hopes to
expand  marketing and  distribution  into Spain,  Turkey and the United  States.
However,  since all discussions with such  distributors are merely  preliminary,
the Company cannot predict when, or even if, it will penetrate such markets. The
Company also anticipates  providing  distributors  with rebates for co-operative
advertising  and freight and discount  allowances.  At this time,  the Company's
only business is the marketing and distribution of the Indicator. The Company is
generating  revenue from the sale of the Indicator in Canada (more  particularly
described  in Item 2 of  this  Amendment  No.  1 to the  Company's  Registration
Statement on Form 10-SB).  The Company has a very limited  operating history and
has not realized significant revenues from its operations.

The  Indicator  will be  targeted  toward:  (i) chain drug  stores and  pharmacy
retailers, (ii) distributors selling to health food chains, and (iii) natural or
homeopathic medical clinics.

Competition.  The Company has identified two significant  competitors,  Personal
Fertility Technologies, Inc. and Med-Direct Products, Inc.

Personal  Fertility  Technologies,  Inc.  ("PFT").  Headquartered in Gold River,
California,  PFT has  designed  a product  called  the PFT  1-2-3TM , which uses
colored slides to incorporate a technique similar to the staining method used in
medical test laboratories.  PFT has distributors in Mexico,  Germany,  Hong Kong
and Canada. The retail price of the PFT 1-2-3 ranges from anywhere from US$89.95
to US$129.95. To the best of the Company's knowledge,  this product has not been
approved by the United  States Food and Drug  Administration,  but is  currently
being re-tested for distribution in the United States.

Med-Direct  Products Inc. ("MDP").  Headquartered in Australia,  MDP distributes
(i) the Lady Fertility  Tester, a saliva-based  fertility test; (ii) the Bioself
Fertility Indicator, a temperature and calendar-based  fertility test; (iii) the
Lady Ovulation Tester, a urine-based fertility test; and (iv) the Lady Pregnancy
Tester, also a urine-based  fertility test. The Lady Fertility Tester is not for
sale in either Canada or the United  States.  In Australia,  the Lady  Fertility
Tester retails for 55 Australian Dollars or approximately US$35.00

The Indicator retails for approximately CDN$40.00,  providing the Company with a
competitive  pricing  advantage.  The Indicator  also requires the purchase of a
CDN$3.00  book of charts per year.  The charts  accompanying  the  Indicator are
provided  free of charge with the  purchase of an  Indicator.  The Company  also
believes that it will have a significant  advantage over the Australian  product
because of the North American Free Trade  Agreement and monetary  exchange rates
favorable  for the  export of  Canadian  products.  The  Company  may reduce its
introductory price to attract distributors.

The Company believes that the Indicator occupies a unique position in the market
for  natural  family  planning  methods.  The Company  believes  that the unique
features  of  the  Indicator  will  allow  it  to  compete  with,  and  in  some
circumstances,  surpass  its  competition.  However,  the Company  will  compete
directly with other  companies and businesses that will have developed or are in
the  process of  developing  products  that will be  competitive  with  products
marketed by the Company.  There can be no assurance that other products that are
functionally  equivalent or similar to the Indicator  have not been developed or
are not in  development.  The  Company  believes  that there are  companies  and
businesses  that exist and may have developed or are developing such products as
well as other  companies  and  businesses  that have the  expertise  that  would
encourage them to develop and market products  directly  competitive  with those
marketed by the Company.  Many of these  competitors have greater  financial and
other  resources,  and more  experience  in research and  development,  than the
Company or its subsidiary. There can be no assurance that the competitors of the
Company  have not or will  not  succeed  in  developing  products  that are more
effective than the Indicator,  or which would render the Indicator  obsolete and
non-competitive.  Many of the


                                       6
<PAGE>

competitors of the Company have substantially greater experience,  technical and
financial resources in production,  marketing and development  capabilities than
the Company.

Natural Family Planning Using the Luna Fertility Indicator.  The health problems
and abortifacient properties associated with pills, IUDs, and Norplant have been
documented  but seldom  disseminated  to  patients.  The Company  believes  that
third-party  tests  indicate the  Indicator  has no side effects that can reduce
fertility in the long-term, and that natural family planning using the Indicator
is a safe natural family planning device.  However, the Company cannot attest to
the accuracy, extent, nature or validity of those third-party tests. The Company
believes  that the use of the  Indicator  is a helpful  and  useful  way to plan
pregnancy.  The Company believes that  approximately  20% of couples  experience
problems  achieving  pregnancy when they want to. The Company  believes that the
Indicator is particularly useful to those women suffering from either reduced or
marginal fertility. The fertility awareness provided by the Indicator allows the
couple to take  advantage  of those  times when the woman is most  fertile.  The
Company  believes  that the  Indicator is based on sound  scientific  knowledge,
helpful  in  assisting  couples  in  understanding  mutual  fertility,   morally
acceptable and easy to learn. The Company believes that the use of the Indicator
and the accompanying  charts will encourage and facilitate couples to (i) follow
each cycle as it unfolds;(ii) understand certain psychological reactions;  (iii)
discern the period of ovulation;  (iv) recognize  possible signs of infertility;
(v) predict  menstruation;  (vi) detect the re-establishment of ovulatory cycles
after taking  contraceptive  pills or after pregnancy;  (vii) promote  conscious
procreation;  (viii) assist them in the choice,  use and means of  contraception
regulation;  and (ix) recognize the approach of menopause.  The Indicator allows
for a couple to track the woman's  fertility  without  chemicals,  mechanical or
surgical means.

Basic Fertility  Awareness.  In a typical  menstrual  cycle, a woman has several
days of bleeding,  usually  followed by a few infertile  days, then several days
during which fertile cervical fluid is produced,  then ovulation.  About 2 weeks
after  ovulation the cycle ends and the bleeding of the next cycle  begins.  The
different  parts of this cycle can be identified by changes in body  temperature
and production of cervical fluid. In the usual cycle,  cervical fluid increases,
ovulation  occurs,  then the  cervical  fluid  dries and basal body  temperature
increases.  An increase in basal body temperature of approximately half a degree
Fahrenheit is a reliable indicator that ovulation has occurred. This increase in
basal body  temperature  remains for  approximately  2 weeks (called the "luteal
phase"), then usually decreases just before menses starts again.

Other  Methods of Natural  Family  Planning.  The now almost  obsolete  Calendar
Rhythm method used each woman's past  menstrual  cycle history to predict future
cycles.  Its  method  effectiveness,  up to  87%,  was  similar  to  that of its
competitors in the 1930's and 1940's. The Ovulation Method ("OM"), also known as
the Billings  method,  depended on  observation  of  menstrual  bleeding and the
production   of   cervical   fluid.    Such   observations   were   subject   to
misinterpretation. Also, in a very short menstrual cycle, fertile cervical fluid
may  begin  to be  produced  before  menstruation  has  finished,  and it may be
difficult to observe in the presence of bleeding.

Using  cervical  fluid  observations  such  as the OM but  cross-checking  those
observations by temperature is called the  Sympto-Thermal  Method  ("STM").  STM
requires daily temperature measurements, taken upon waking in the morning at the
same time every day. It also relies on symptoms of fertility,  most commonly the
presence of fertile cervical fluid,  and the position of the cervix.  Around the
fertile time, the cervix withdraws  further into the body and the opening of the
cervix increases. At the time of ovulation, temperature starts to increase about
half a degree Fahrenheit.  Cross-checked with the other symptoms,  this provides
confirmation  that ovulation is occurring and then determines the infertile time
following ovulation.

Recently,  researchers  have  defined  what they call the  Lactation  Amenorrhea
Method  ("LAM").  After giving  birth,  a woman  normally  experiences a time of
infertility  until her body is ready for another  pregnancy.  If a woman doesn't
breastfeed,  this  period of  infertility  is usually  quite  short.  If a woman
exclusively  breastfeeds,  without pacifiers,  bottles or schedules, the average
length of  infertility  is 14 months,  but can vary from a few months to several
years.

Employees.  The  Company  does not  currently  have any  employees.  The Company
currently  uses the services of three  consultants  at its  corporate  office in
Vancouver,  British  Columbia.  Campbell Capital  Advisory,  Inc.,  provides the
services  of Gordon  McDougall,  President  and Chief  Executive  Officer of the
Company, for management and


                                       7
<PAGE>

administrative  services  to the  Company.  Melissa  Gervais  provides  in-house
marketing and sales services to the Company.  Glen Wallace  supplies  accounting
and financial consulting services on a month-to-month, as needed basis.

Reports to Security Holders.  The Company intends to provide an annual report to
its security  holders,  which will include  audited  financial  statements.  The
Company  will  become a  reporting  company  with the  Securities  and  Exchange
Commission  ("SEC") upon the effective  date of this  Registration  Statement on
Form 10-SB,  at which time the public may read and copy any materials filed with
the SEC at the SEC's Public Reference Room at 450 Fifth Street N.W., Washington,
D.C.  20549.  The public may also obtain  information  on the  operation  of the
Public Reference Room by calling the SEC at 1-800-SEC-0330. The SEC maintains an
Internet site that contains reports, proxy and information statements, and other
information regarding issuers that file electronically with the SEC. The address
of that site is http://www.sec.gov.

Item 2. Management's  Discussion and Analysis of Financial Condition and Results
of Operations

Revenue. The Company's year end is March 31 and its first year end was March 31,
1999.  For the first  fiscal  year,  which  covered  the period from the date of
incorporation on January 19, 1999 to March 31, 1999, the Company generated gross
revenue  of  US$1,020  from sales of the  Indicator,  and an  operating  loss of
approximately  US$29,100. For the first fiscal quarter, which covered the period
from April 1, 1999 to June 30, 1999, the Company  generated revenue of US$15,547
from sales of the Indicator.  For that same period,  the Company  experienced an
operating  loss of  approximately  US$70,200.  The  following  chart  represents
historical sales of the Indicator.

                                Schedule of Sales
                        January 19, 1999 to June 30, 1999

================================================================================
Month                         Sales                                 Units Sold
================================================================================
January 1999                          US$0                                    0
- --------------------------------------------------------------------------------
February 1999                         US$0                                    0
- --------------------------------------------------------------------------------
March 1999                        US$1,020                                   75
- --------------------------------------------------------------------------------
April 1999                        US$1,061                                   77
- --------------------------------------------------------------------------------
May 1999                         US$13,187                                  798
- --------------------------------------------------------------------------------
June 1999                         US$1,299                                   32
================================================================================

Costs and  Expenses.  Cost of sales for the fiscal  year ended  March 31,  1999,
represented 81.1% of revenues. For the first fiscal quarter ended June 30, 1999,
these costs  represented 59.7% of that period's  comparatively  higher revenues.
The Company believes the higher  proportion of cost of sales for the fiscal year
ended March 31, 1999, was the result of the commencement of initial sales of the
Indicator,  and the lower proportion  during the first fiscal quarter ended June
30, 1999, is more indicative of the anticipated revenue to cost ratio.

Consulting  fees of US$13,163  represented  the largest  single  expense for the
fiscal  year  ended  March 31,  1999 and  consisted  of  US$8,163  for  in-house
marketing  services and US$5,000 for  management  fees paid to Campbell  Capital
Advisory,  Inc. (see Item 7). For the first fiscal  quarter ended June 30, 1999,
consulting  fees  totaled  US$11,437  which was the direct  result of  increased
marketing  activity  related  to the  Indicator.  Management  fees of  US$15,000
accrued to Campbell  Capital  Advisory,  Inc., were disclosed  separately in the
first fiscal quarter's financial statements.

Marketing expenses totaled US$5,907 for the fiscal year ended March 31, 1999 and
US$24,787 for the first fiscal quarter ended June 30, 1999,  which resulted from
increased marketing activity relating to the Indicator.

Liquidity  and Capital  Resources.  Net cash used for operating  activities  was
US$27,071 for the fiscal year ended March 31, 1999,  and US$32,038 for the first
fiscal quarter ended June 30, 1999.  The net cash used for operating


                                       8
<PAGE>

activities during fiscal year ended March 31, 1999,  consisted  primarily of the
net loss of  US$29,097  during the  development  stage and  increases in prepaid
expenses, accounts payable and accrued liabilities.  Net cash used by operations
during the first fiscal quarter ended June 30, 1999  consisted  primarily of the
net loss of  US$70,232  and was offset to an extent by an  increase  in accounts
payable and accrued liabilities of US$37,278.

Net cash used by investing  activities  was  US$40,001 for the fiscal year ended
March 31, 1999. During this period,  the Company advanced a loan of US$40,000 to
Luna Products,  Inc., pursuant to the agreement to acquire the worldwide license
to distribute the Luna Fertility  Indicator,  as described in Item 1. During the
first fiscal quarter ended June 30, 1999, net cash used by investing  activities
totaled US$710.

Net cash  provided by financing  activities  totaled  US$76,969  for fiscal year
ended March 31, 1999, of which US$72,500 came from the sale of 7,310,660  shares
of the Company's  common stock. A further  US$20,469 came from short-term  loans
from Campbell  Capital  Advisory,  Inc.,  the sole  shareholder  of which is Mr.
Gordon McDougall, President, Chief Executive Officer and director of the Company
(see Item 7).  During  the  period,  US$16,000  of these  short-term  loans were
repaid.  During the first fiscal  quarter ended June 30, 1999, net cash provided
by financing  activities  totaled  US$27,337.  Of this total,  additional  loans
totaling  US$5,398 were advanced by Campbell  Capital  Advisory,  Inc.,  and the
Company received short term loans totaling  US$16,939 from Javelin  Enterprises.
None of the  officers or directors  of the Company are  affiliated  with Javelin
Enterprises; as such, the loan to the Company was at arm's-length. The loan from
Campbell  Capital  Advisory,  Inc., is  unsecured,  bears no interest and has no
fixed terms of  repayment,  and is to be repaid as funds become  available.  The
loan from Javelin  Enterprises bears interest at ten percent (10%) per annum and
is due and  payable on or before  June 2, 2000.  The  Company  has the option to
repay the loan to Javelin Enterprises prior to June 2, 2000, without penalty.

As at March 31,  1999 and June 30,  1999,  the  Company  had cash  resources  of
US$9,897  and  US$4,486,  respectively,  the  latter  of which  constitutes  the
Company's  present  internal  sources  of  liquidity.  Because  the  Company  is
generating  only limited  revenues from the sale of the Indicator  product,  the
Company's main external source of liquidity is the sale of its capital stock.

The Company,  being a developmental stage enterprise,  is currently focusing its
efforts on the marketing and sale of the  Indicator  which will, if  successful,
mitigate the net loss  experienced by the Company.  The Company is reviewing its
options to raise substantial equity capital. Management has proceeded as planned
in the ongoing  development,  marketing and sale of the  Indicator.  In order to
satisfy its  requisite  budget,  management  has held and  continues  to conduct
negotiations with potential investors. The Company hopes that these negotiations
will result in  significant  investment in the Company.  To achieve and maintain
its  competitiveness  of the Indicator and to conduct costly and  time-consuming
marketing  and  promotional  activities,  the  Company  may be required to raise
additional funds in addition to the funds already raised through the issuance of
the Company's  shares and through the  realization of limited revenue from sales
of the  Indicator.  The Company's  forecast for the period of time through which
its  financial  resources  will be  adequate  to  support  its  operations  is a
forward-looking  statement  that involves  risks and  uncertainties,  and actual
results could fail as a result of a number of factors.  The Company  anticipates
that it will need to raise  additional  capital in order to promote,  market and
distribute the Indicator.  Such additional  capital may be raised through public
or private financings as well as other borrowings and other resources.

The Company  believes that its current cash  resources,  coupled with  projected
revenue from sales of the Indicator and capital received from additional  public
or  private  financings,  as well as  borrowings  and other  resources,  will be
sufficient to support its operations  during the next  12-months.  However,  the
Company  cannot  guarantee  that any one source of  capital,  by itself,  or all
projected  sources  combined,  will be sufficient to support its operations over
the next 12-months. Moreover, there can be no assurances that additional funding
will be available  under  favorable  terms, if at all. If adequate funds are not
available, the Company may be required to curtail operations significantly or to
obtain funds by entering into  arrangements with  collaborative  partners or may
require the Company to relinquish rights to the Indicator that the Company would
not  otherwise  relinquish.  However,  the  Company  believes  its is  poised to
maintain both its short-term and its long-term  liquidity.  The Company believes
that it can continue to successfully market and sell the Indicator.


                                       9
<PAGE>

Results of  Operations.  The Company did not realize  significant  revenue  from
sales of the Indicator from January 19, 1999  (inception) to March 31, 1999. The
Company did realize gross revenue of US$1,020 for that period, and US$15,547 for
the first  fiscal  quarter  ended  June 30,  1999 from  sales of the  Indicator.
However,  the Company was  incorporated  on January 19, 1999, and as such has no
significant  operating  history upon which an estimate of future earnings can be
based.

Year 2000 Compliance. Historically, certain computer programs were written using
two digits  rather than four to define the  applicable  year.  Accordingly,  the
Company's  software could  recognize the date using "00" as 1900 rather than the
Year 2000,  which could  result in major  systems  failures  or  miscalculations
commonly  referred to as the Year 2000  issue.  The  Company  has  performed  an
assessment of its information technology systems of the Company and expects that
all necessary  modifications  and necessary  replacements will be completed in a
timely  manner to  ensure  the  systems  are Year 2000  compliant.  The  Company
currently  utilizes  only two  personal  computers.  Based  upon  the  Company's
estimates,  the cost of  addressing  the Year 2000  issue as it  relates  to the
Company's  computers are not expected to have a material  adverse  effect on the
Company's  financial  situation,  results  of  operations  or  cash  flows.  The
potential  impact of the Year 2000 issue on  significant  customers,  vendors or
suppliers  of the  Company  cannot be  reasonably  estimated  at this time.  The
Company is not yet certain as to the extent to which the  computer  software and
business  systems of its customers and  suppliers  are Year 2000  compliant.  If
systems of third  parties with which the Company does  significant  business are
not timely  converted or, if the Company fails to timely  complete the necessary
modifications  to its own  systems,  the Year 2000  issue  could have a material
adverse  effect on the  Company's  business,  financial  conditions,  results of
operations and cash flows.  The Company's  contingency plan is to routinely back
up its computer  information  off of the two computers  the Company  utilizes in
order to ensure that the information is not lost should the Year 2000 issue have
a material  effect on the Company's  computer  system.  The cost incurred by the
Company to address the Year 2000 issue has been de-minimus.

Item 3. Description of Property

Property held by the Company. The Company does not own any significant property.

The Company's  Facilities.  The Company  occupies  facilities  consisting of 600
square feet of commercial  office space located at 1820-1095 West Pender Street,
Vancouver,  British Columbia, V6E 2M6. The office space is furnished by Campbell
Capital Advisory, Inc., located in premises rented to Campbell Capital Advisory,
Inc., by International Parkside on a month-to-month basis. From January 19, 1999
(inception)  through the period  ending March 31, 1999,  the Company had paid to
International  Parkside a total of US$1,700 rent. During the three-month  period
ended June 30,  1999,  the  Company  paid to  International  Parkside a total of
US$1400 rent.

The  Company  also rents,  on an  as-needed  basis,  storage and work space from
Melissa Gervais for US$400 a month. From January 19, 1999  (inception),  to June
30, 1999, the Company had paid US$1600 to Ms. Gervais.

Item 11. Description of Securities

The Company is authorized to issue  50,000,000  shares of common stock,  US$.001
par value,  each share of common  stock  having  equal  rights and  preferences,
including voting  privileges;  and 5,000,000 shares of preferred stock,  US$.001
par value.  As of June 30, 1999,  there were  7,310,660  shares of the Company's
common stock were issued and outstanding, and no shares of the Company's US$.001
par value  preferred  stock issued and  outstanding.  As of March 31, 1999,  the
Company  had  received a total of  US$72,500  as  proceeds  from the sale of its
common stock  pursuant to the offerings  described in Item 10 of this  Amendment
No. 1 to the Company's  10-SB. On or about April 15, 1999, the Company  received
US$5,000  as  money  owed  on the  sale  of its  common  stock  pursuant  to the
above-referenced offerings. The receipt of this sum is reflected in the attached
financial  statements  for the period ended June 30, 1999,  as "Receipt of stock
subscriptions receivable".

The shares of US$.001 par value  common stock of the Company  constitute  equity
interests in the Company  entitling each shareholder to a pro rata share of cash
distributions made to shareholders, including dividend payments. The


                                       10
<PAGE>

Bylaws of the Company specify how the cash available for  distribution,  whether
occurring  from  operations or sales or  refinancing,  is to be shared among the
shareholders. The holders of the Company's common stock are entitled to one vote
for each share of record on all matters to be voted on by shareholders. There is
no cumulative voting with respect to the election of directors of the Company or
any other  matter,  with the result that the holders of more than fifty  percent
(50%) of the shares voted for the election of those  directors  can elect all of
the directors. The holders of the Company's common stock are entitled to receive
dividends  when,  as and if declared by the  Company's  Board of Directors  from
funds legally available therefore; provided, however, that cash dividends are at
the sole  discretion  of the  Company's  Board  of  Directors.  In the  event of
liquidation,  dissolution  or winding up of the  Company,  the holders of common
stock are  entitled  to share  ratably in all  assets  remaining  available  for
distribution  to them after  payment of  liabilities  of the  Company  and after
provision has been made for each class of stock,  if any,  having  preference in
relation to the Company's US$.001 par value common stock.  Holders of the shares
of Company's common stock have no conversion,  preemptive or other  subscription
rights,  and there are no  redemption  provisions  applicable  to the  Company's
common stock.

Item 15. Financial Statements and Exhibits

(b) Index to Exhibits                                 Page
- ---------------------                                 ----

Specimen Stock Certificate                            E-1 through E-2


                                       11
<PAGE>

                                   SIGNATURES

In accordance  with the provisions of Section 12 of the Securities  Exchange Act
of 1934, Luna Medical Technologies, Inc. has duly caused this Amendment No. 2 to
the  Registration  Statement  on Form  10-SB to be signed  on its  behalf by the
undersigned, thereunto duly authorized, in the City of             , on November
22, 1999.

                                       Luna Medical Technologies, Inc.,
                                       a Nevada corporation

                                       By:  /s/ Gordon McDougall
                                            ----------------------------------
                                            Gordon McDougall
                                       Its: President


                                       12



  COMMON STOCK                                                    COMMON STOCK

- ----------------                                                ----------------
                             LUNA TECHNOLOGIES INC.
- ----------------                                                ----------------
                                    SPECIMEN



INCORPORATED UNDER THE LAWS OF                              SEE REVERSE FOR
     THE STATE OF NEVADA                                  CERTAIN DEFINITIONS

                                                           CUSIP 55036M 10 3

================================================================================

THIS CERTIFIES THAT






IS THE RECORD HOLDER OF

================================================================================


FULLY PAID AND NONASSESSABLE SHARES OF THE COMMON STOCK, $.001 PAR VALUE, OF
                             LUNA TECHNOLOGIES INC.

transferable  on the books of the  corporation  in person or by duly  authorized
attorney upon surrender of this Certificate properly endorsed.  This Certificate
is not valid unless  countersigned  and  registered  by the  Transfer  Agent and
Registrar.

     WITNESS the facsimile seal of the corporation  and the facsimile  signature
     of its duly authorized officers.



CERTIFICATE OF STOCK



Dated:


  /s/ G. McDougall              [CORPORATE SEAL]             /s/ G. McDougall
                             Luna Technologies, Inc.
    SECRETARY                        1999                        PRESIDENT
                                    NEVADA
                                       *


COUNTERSIGNED AND REGISTERED:
     U.S. STOCK TRANSFER CORPORATION
          TRANSFER AGENT AND REGISTRAR


BY
   -----------------------------------
         AUTHORIZED SIGNATURE

<PAGE>

     The following  abbreviations,  when used in the  inscription on the face of
this  certificate,  shall be  construed  as though they were written out in full
according to applicable laws or regulations:


TEN COM - as tenants in common
TEN ENT - as tenants by the [illegible]
JT TEN - as joint tenants with right of
         survivorship and not as tenants
         in common

UNIF GIFT MIN ACT  -   _____________ Custodian ___________
                       ([illegible])            (author)
                       under Uniform Gifts to Minors
                       Act________________________________
                                    (State)

UNIF GIFT MIN ACT  -   _____________ Custodian (until age _______)
                       ([illegible])
                       _______________ under Uniform Transfers
                          (minor)
                       to Minors Act..,    _____________________
                                                  (State)


    Additional abbreviations may also be used though not in the above list.


FOR VALUE RECEIVED, _____________________ hereby sell, assign and transfer unto

PLEASE INSERT SOCIAL SECURITY OR OTHER
    IDENTIFYING NUMBER OF ASSIGNEE
- --------------------------------------

- --------------------------------------


- --------------------------------------------------------------------------------
  (PLEASE PRINT OR TYPEWRITE NAME AND ADDRESS, INCLUDING ZIP CODE OF ASSIGNEE)

- --------------------------------------------------------------------------------

- --------------------------------------------------------------------------------

                                                                        Shares
- -----------------------------------------------------------------------
 of the common stock represented by the within Certificate, and do
             hereby irrevocably constitute and appoint

                                                                       Attorney
- -----------------------------------------------------------------------
to transfer the said stock on the books of the within named Corporation
            with full power of substitution in the premises.


Dated ____________________________



                                       X
                                         ---------------------------------------

                                       X
                                         ---------------------------------------
                                 NOTICE: THE SIGNATURES TO THIS ASSIGNMENT MUST
                                         CORRESPOND WITH THE NAME(S) AS WRITTEN
                                         UPON THE FACE OF THE CERTIFICATE IN
                                         EVERY PARTICULAR, WITHOUT ALTERATION OR
                                         ENLARGEMENT OR ANY CHANGE WHATEVER.

Signature(s) Guaranteed



By _____________________________________
THE SIGNATURE(S) MUST BE GUARANTEED
BY AN ELIGIBLE GUARANTOR INSTITUTION
(BANKS, STOCKBROKERS, SAVINGS AND LOAN
ASSOCIATIONS AND CREDIT UNIONS WITH
MEMBERSHIP IN AN APPROVED SIGNATURE
GUARANTEE [ILLEGIBLE] PROGRAM, PURSUANT
TO [ILLEGIBLE] RULE 17 ACT 15.



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