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Femasys Announces Financial Results for Quarter Ended September 30, 2026 and Provides Corporate Update

(Moderate)

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Femasys (NASDAQ: FEMY) reported third-quarter sales of $404,597, down 44.5% year over year, alongside a wider net loss. U.S. sales rose to $347,039 from $336,594. Net loss reached $4,564,815 versus $4,194,821, while loss per share narrowed to $0.53 from $2.05. Nine-month sales fell 21.5% to $1,161,313, and net loss narrowed to $8,187,810 from $14,677,582.

A completed $30 million private placement supports U.S. commercial hiring and the FemBloc pivotal trial. Total proceeds could reach up to $85 million upon full cash exercise of warrants. Cash was $23,913,946 at September 30, 2026, versus $9,266,353 at December 31, 2025. FemBloc received FDA approval for a modular premarket approval submission approach, and actively enrolling FINALE trial sites doubled to twelve. New patents cover its blended polymer component. Femasys also announced fertility portfolio partnerships with UNC Health and Minnesota Women’s Care.

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20 points · 1 major

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1 major · 14 points

Hollow bars mark forward-looking points. How the balance works

Positive

  • Major pointCompleted $30 million private placement funds U.S. commercial team expansion and the FemBloc pivotal trial. 2.6× market cap
  • Moderate pointNine-month net loss narrowed to $8,187,810 from $14,677,582; loss per share narrowed to $1.59 from $9.25.
  • Moderate pointFDA approval permits a modular premarket approval submission approach for FemBloc.
  • Minor point. Forward-looking: it has not happened yet and may not happen.Potential total financing proceeds reach up to $85 million upon full cash exercise of warrants.
  • Minor pointCash and cash equivalents rose to $23,913,946 at September 30, 2026, from $9,266,353 at December 31, 2025.
15 minor points
  • Minor pointQ3 U.S. sales increased to $347,039 from $336,594 a year earlier.
  • Minor pointNine-month U.S. sales increased to $1,038,997 from $1,015,168 a year earlier.
  • Minor pointFINALE actively enrolling trial sites doubled to twelve to support FemBloc U.S. approval.
  • Minor pointFemBloc patents issued in U.S. and international markets expand protection for the blended polymer component.
  • Minor point. Forward-looking: it has not happened yet and may not happen.Commercial recruitment is underway following financing; Femasys expects territorial deployment to broaden adoption and drive revenue growth.
  • Minor pointNine-month research and development expenses decreased 9.8% to $5,199,206 from $5,764,923.
  • Minor pointQ3 sales and marketing expenses declined to $943,002 from $1,143,805 a year earlier.
  • Minor pointCost of sales, excluding depreciation fell year over year: Q3 to $187,496 from $293,838; nine months to $488,538 from $569,275.
  • Minor pointInterest expense fell year over year: Q3 to $200,415 from $532,073; nine months to $563,072 from $1,483,022.
  • Minor pointInterest income rose year over year: Q3 to $85,610 from $17,315; nine months to $155,131 from $53,488.
  • Minor pointNine-month fair-value gains were $1,732,413 on the conversion option liability and $4,228,000 on warrant liabilities.
  • Minor pointDepreciation and amortization declined year over year: Q3 to $77,091 from $85,697; nine months to $242,172 from $256,835.
  • Minor pointOther expense fell to zero in Q3 and nine months, versus $26,295 and $286,295, respectively, a year earlier.
  • Minor pointTotal liabilities declined to $8,059,496 at September 30, 2026, from $14,854,875 at December 31, 2025.
  • Minor pointStockholders’ equity increased to $27,028,162 at September 30, 2026, from $5,869,302 at December 31, 2025.

Negative

  • Major pointCommon shares outstanding increased to 8,656,277 at September 30, 2026, from 2,980,254 at December 31, 2025.
  • Moderate pointQ3 sales declined 44.5% year over year to $404,597 from $729,394.
  • Moderate pointQ3 net loss widened to $4,564,815 from $4,194,821, although loss per share narrowed to $0.53 from $2.05.
  • Minor pointNine-month sales declined 21.5% year over year to $1,161,313 from $1,479,926.
  • Minor point. Forward-looking: it has not happened yet and may not happen.Financing warrants create potential additional dilution if exercised.
9 minor points
  • Minor pointQ3 research and development expenses increased 40.6% to $1,942,927 from $1,382,022.
  • Minor pointNine-month sales and marketing expenses increased to $3,552,755 from $3,037,349 a year earlier.
  • Minor pointGeneral and administrative expenses rose year over year: Q3 to $1,704,091 from $1,477,800; nine months to $5,418,059 from $4,817,485.
  • Minor pointOperating losses widened year over year: Q3 to $4,450,010 from $3,653,768; nine months to $13,739,417 from $12,965,941.
  • Minor point. Forward-looking: it has not happened yet and may not happen.International FemBloc reorders are expected after distributors complete post-market studies using existing inventory.
  • Minor pointConvertible notes payable, net rose to $3,717,653 at September 30, 2026, from $3,178,864 at December 31, 2025.
  • Minor pointCurrent note payable reached $292,229 at September 30, 2026, versus none at December 31, 2025.
  • Minor pointAccumulated deficit increased to $154,013,954 at September 30, 2026, from $145,826,144 at December 31, 2025.
  • Minor pointNine-month income taxes shifted to $865 expense from a $4,188 benefit a year earlier.

News Explained

The balance sheet reports 8,656,277 common shares outstanding on September 30, 2026, versus 2,980,254 on December 31, 2025; issuing additional shares increases the total share count and reduces existing holders’ percentage ownership absent offsetting changes.

Key Figures

Completed private placement: $30 million Potential warrant proceeds: Up to $85 million Q3 overall sales: 44.5% decrease to $404,597 from $729,394 +5 more
Completed private placement
$30 million
Completed in mid-August 2026
Potential warrant proceeds
Up to $85 million
Upon full cash exercise of warrants
Q3 overall sales
44.5% decrease to $404,597 from $729,394
Quarter ended September 30, year over year
Q3 U.S. sales
$347,039 from $336,594
Quarter ended September 30, year over year
Q3 net loss
$4,564,815 from $4,194,821
Quarter ended September 30, year over year
Nine-month net loss
$8,187,810 from $14,677,582
Nine months ended September 30, year over year
Cash and cash equivalents
Approximately $23.9 million
As of September 30, 2026
Actively enrolling FINALE sites
12 sites, doubled
FemBloc pivotal trial

Previous Earnings Reports

3 past events · Latest: Aug 14
Same Type 3 events
  1. Aug 14

    Earnings and financing

    24h Move
    -5.7%

    Completed $30 million placement; six-month sales rose and net loss narrowed.

  2. May 08

    Quarterly earnings

    24h Move
    -6.0%

    Q1 sales increased, with net income and early FemaSeed adoption reported.

  3. Nov 14

    Quarterly earnings

    24h Move
    -11.3%

    Q3 sales increased year over year alongside regulatory milestones and financing.

24h Move is the share-price change in the day after each event; other market factors may also have contributed.

Key Terms

private placement, warrants, pivotal trial, premarket approval, +1 more
5 terms
private placement financial
"Completed $30 million private placement"
A private placement is a sale of securities directly to a selected group of investors, typically institutions or accredited investors, instead of through a public offering. It lets a company raise money faster and with fewer regulatory steps; for existing shareholders it matters because the newly issued shares, often sold at a discount, increase the share count and can dilute their ownership.
warrants financial
"upon full cash exercise of warrants"
Warrants are special documents that give you the right to buy a company's stock at a set price before a certain date. They are often used as a way for companies to attract investors or raise money, and their value can increase if the company's stock price goes up.
View in glossary
pivotal trial medical
"to fund the FemBloc® pivotal trial"
A pivotal trial is a key test of a new medicine or treatment to see if it works and is safe enough to be approved by health authorities. It's like a final exam for a new product, and passing it is essential for bringing the treatment to the public.
premarket approval regulatory
"FDA approval of the modular premarket approval (PMA) submission approach"
Premarket approval is the formal regulatory clearance required before certain medical devices can be sold, based on detailed evidence that the product is safe and effective. For investors, it’s a major milestone because receiving approval typically clears the way for commercial sales and reduces regulatory uncertainty, while failure or delays can block revenue and raise the risk profile; think of it like a safety certificate needed before a new car model can be sold.
post-market studies medical
"utilizing existing inventory to support FemBloc post-market studies"
Studies conducted after a medical product or device has been approved and is being sold, aimed at tracking real-world safety, effectiveness, and long-term performance. They matter to investors because their results can trigger regulatory actions, label changes, additional costs, or reputational effects—similar to ongoing vehicle safety checks that can lead to recalls or software updates and influence a company’s future sales and legal exposure.

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$30 million private placement supports commercial team build-out to drive U.S. sales growth; Q3 U.S. sales increased slightly despite significant funding constraints prior to mid-August financing

ATLANTA, Nov. 13, 2026 (GLOBE NEWSWIRE) -- Femasys Inc. (NASDAQ: FEMY), a leading biomedical innovator developing transformative fertility and non-surgical permanent birth control solutions designed to improve the standard of care, expand access, and reduce costs for women worldwide, announces its financial results for the quarter ended September 30, 2026 and provides a corporate update.

Corporate Highlights from 3Q 2026 to date

  • Completed $30 million private placement with potential total proceeds of up to $85 million upon full cash exercise of warrants, to build-out the U.S. commercial team needed to support revenue growth following recent availability of the FemaSeed® fertility portfolio to OB/GYNs, and to fund the FemBloc® pivotal trial to support U.S. approval.
  • Highlights for the FemaSeed Fertility Portfolio (Diagnostics: FemVue® for her and SpermVueTM for him; first-step treatment: FemaSeed and FemSperm®):
    • Announced a partnership with both UNC Health and Minnesota Women’s Care to introduce the entire portfolio across its OB/GYN practice locations.
    • Announced a partnership with CapexMD to expand patient access through financing solutions and SandsRx Pharmacy for medications to support treatment timing.
  • Highlights for FemBloc Permanent Birth Control:
    • Issuance of patents in the U.S. and key international markets that expand intellectual property protection for the blended polymer component.
    • Received FDA approval of the modular premarket approval (PMA) submission approach.
    • Announced the number of actively enrolling sites in the FINALE trial to support U.S. approval doubled to twelve sites.

“We maintained a lean team and tightly managed resources as we prioritized financing from long-term institutional investors. Closing the $30 million in financing in mid-August 2026 represents an important turning point for Femasys,” said Kathy Lee-Sepsick, Founder and Chief Executive Officer of Femasys. “With U.S. fertility rates at historic lows, there is an urgent need to bring treatment to the OB/GYN office, where women already seek care. Our portfolio enables these physicians to offer a complete pathway from diagnostics through first-step treatment, supported by partnerships that simplify access to patient financing and fertility medications. Since closing the financing, we have been successfully recruiting commercial professionals with deep OB/GYN expertise and established relationships. Healthcare system partnerships and initial sales achieved with limited resources demonstrate the commercial potential of our comprehensive fertility portfolio. These results and commercial recruitment progress give us strong confidence that deploying our team in target U.S. territories will broaden adoption and drive revenue growth.”

Financial Results for Quarter Ended September 30, 2026

  • Sales in the U.S. increased slightly to $347,039 in 2026 from $336,594 in 2025, while overall sales decreased by $324,797, or 44.5%, to $404,597 from $729,394. The overall decline was anticipated and reflects the timing of international FemBloc orders, consistent with distributors’ customary bulk-ordering practices. Distributors are utilizing existing inventory to support FemBloc post-market studies, with reorders expected after those studies are completed.
  • Research and development expenses increased by $560,905, or 40.6%, to $1,942,927 in 2026 compared to $1,382,022 in 2025, primarily reflecting the transition of development products into inventory to support commercialization during 2025, and increased clinical costs and compensation costs during 2026.
  • Net loss was $4,564,815, or ($0.53) per basic and diluted share attributable to common stockholders, for the quarter ended September 30, 2026, compared to a net loss of $4,194,821, or ($2.05) per basic and diluted share attributable to common stockholders, for the quarter ended September 30, 2025.

Financial Results for Nine Months Ended September 30, 2026

  • Sales in the U.S. increased slightly to $1,038,997 in 2026 from $1,015,168 in 2025, while overall sales decreased by $318,613, or 21.5%, to $1,161,313 from $1,479,926. The overall decline was anticipated and reflects the timing of international FemBloc orders, consistent with distributors’ customary bulk-ordering practices. Distributors are utilizing existing inventory to support FemBloc post-market studies, with reorders expected after those studies are completed.
  • Research and development expenses decreased by $565,717, or 9.8%, to $5,199,206 in 2026 compared to $5,764,923 in 2025, primarily reflecting lower compensation costs, regulatory fees and outside consultant costs, partially offset by increased clinical costs and material and development costs.
  • Net loss was $8,187,810, or ($1.59) per basic and diluted share attributable to common stockholders, for the nine months ended September 30, 2026, compared to a net loss of $14,677,582, or ($9.25) per basic and diluted share attributable to common stockholders, for the nine months ended September 30, 2025.
  • Cash and cash equivalents as of September 30, 2026, were approximately $23.9 million and the Company had an accumulated deficit of approximately $154.0 million.

For more information, please refer to the Company’s Form 10-Q filed November 13, 2026, which can be accessed on the SEC website.

 
FEMASYS INC.
Condensed Balance Sheets
(unaudited)
          
Assets September 30,
2026
 December 31,
2025
Current assets:    
 Cash and cash equivalents$23,913,946  9,266,353 
 Accounts receivable, net 233,778  616,600 
 Inventory
 6,166,371  5,740,249 
 Prepaid and other current assets 893,098  833,133 
     Total current assets 31,207,193  16,456,335 
Property and equipment, at cost:    
 Leasehold improvements 1,238,886  1,238,886 
 Office equipment 91,610  78,155 
 Furniture and fixtures 424,586  417,876 
 Machinery and equipment 3,125,855  3,065,713 
 Construction in progress 991,124  897,885 
       5,872,061  5,698,515 
Less accumulated depreciation (3,991,222) (3,802,940)
     Net property and equipment 1,880,839  1,895,575 
Long-term assets:    
 Lease right-of-use assets, net 952,796  1,297,121 
 Intangible assets, net of accumulated amortization 99,902  134,914 
 Other long-term assets 946,928  940,232 
     Total long-term assets 1,999,626  2,372,267 
     Total assets$35,087,658  20,724,177 
(continued)
    
          


 
FEMASYS INC.
Condensed Balance Sheets
(unaudited)
 
Liabilities and Stockholders’ Equity September 30,
2026
 December 31,
2025
Current liabilities:    
 Accounts payable$1,958,546  1,830,124 
 Accrued expenses 855,377  1,265,773 
 Note payable 292,229  — 
 Clinical holdback – current portion 29,250  52,644 
 Operating lease liabilities – current portion 465,960  487,624 
     Total current liabilities 3,601,362  3,636,165 
Long-term liabilities:    
 Clinical holdback – long-term portion 58,179  52,370 
 Convertible notes payable, net 3,717,653  3,178,864 
 Conversion option liability —  2,014,000 
 Warrants liabilities —  4,943,000 
 Operating lease liabilities – long-term portion 682,302  1,030,476 
     Total long-term liabilities 4,458,134  11,218,710 
     Total liabilities 8,059,496  14,854,875 
Commitments and contingencies    
Stockholders’ equity:    
 Common stock, $0.001 par, 200,000,000 shares authorized,    
  8,662,139 shares issued and 8,656,277 shares outstanding as of  
  September 30, 2026; and 2,986,116 shares issued    
  and 2,980,254 shares outstanding as of December 31, 20258,662  2,986 
 Treasury stock, 5,862 common shares (60,000) (60,000)
 Warrants
 19,023,695  5,246,150 
 Additional paid-in capital 162,069,759  146,506,310 
 Accumulated deficit (154,013,954) (145,826,144)
     Total stockholders’ equity 27,028,162  5,869,302 
     Total liabilities and stockholders' equity$35,087,658  20,724,177 
          


FEMASYS INC.
Condensed Statements of Operations
(unaudited)
     
       Three Months Ended September 30, Nine Months Ended September 30,
       2026
 2025
 2026
 2025
Sales   $404,597  729,394  1,161,313  1,479,926 
Cost of sales (excluding depreciation expense) 187,496  293,838  488,538  569,275 
              
Operating expenses:        
 Research and development 1,942,927  1,382,022  5,199,206  5,764,923 
 Sales and marketing 943,002  1,143,805  3,552,755  3,037,349 
 General and administrative 1,704,091  1,477,800  5,418,059  4,817,485 
 Depreciation and amortization 77,091  85,697  242,172  256,835 
     Total operating expenses 4,667,111  4,089,324  14,412,192  13,876,592 
     Loss from operations (4,450,010) (3,653,768) (13,739,417) (12,965,941)
Other income (expense):        
 Interest income 85,610  17,315  155,131  53,488 
 Change in fair value of Conversion Option liability —  —  1,732,413  — 
 Change in fair value of Warrants liabilities —  —  4,228,000  — 
 Interest expense (200,415) (532,073) (563,072) (1,483,022)
 Other expense —  (26,295) —  (286,295)
     Total other income (expense), net (114,805) (541,053) 5,552,472  (1,715,829)
     Loss before income taxes (4,564,815) (4,194,821) (8,186,945) (14,681,770)
 Income tax expense (benefit) —  —  865  (4,188)
     Net loss$(4,564,815) (4,194,821) (8,187,810) (14,677,582)
              
Net loss attributable to common stockholders$(4,564,815) (4,194,821) (8,187,810) (14,677,582)
              
Basic and diluted loss per share$(0.53) (2.05) (1.59) (9.25)
              
Weighted-average common shares and pre-funded warrants outstanding, basic and diluted 8,660,381  2,050,761  5,136,109  1,586,992 
              

About Femasys Inc.
Femasys is a leading biomedical innovator developing transformative fertility and non-surgical permanent birth control solutions designed to improve the standard of care, expand access, and reduce costs for women worldwide. The Company is focused on commercializing its fertility portfolio, led by FemaSeed® Intratubal Insemination, together with complementary diagnostic and sperm preparation products, in the U.S. and key international markets. Femasys is also advancing FemBloc®, its non-surgical, in-office permanent birth control solution, toward U.S. FDA approval through the ongoing FINALE pivotal trial (NCT05977751). FemBloc received regulatory approvals in Europe, the UK and New Zealand in 2025, supporting commercialization through strategic partnerships in select international markets. Femasys’ portfolio is supported by broad intellectual property protection and clinical data demonstrating favorable safety, encouraging effectiveness results, and high patient and practitioner satisfaction.

Learn more at www.femasys.com, or follow us on X, Facebook and LinkedIn.

Forward-Looking Statements 
This press release contains forward-looking statements that are subject to substantial risks and uncertainties. Forward-looking statements can be identified by terms such as “may,” “will,” “should,” “expect,” “plan,” “anticipate,” “could,” “pending,” “intend,” “believe,” “suggests,” “potential,” “hope,” or “continue” or the negative of these terms or other similar expressions, although not all forward-looking statements contain these words. Forward-looking statements are based on our current expectations and are subject to inherent uncertainties, risks and assumptions, many of which are beyond our control, difficult to predict and could cause actual results to differ materially from what we expect. Further, certain forward-looking statements are based on assumptions as to future events that may not prove to be accurate. Factors that could cause actual results to differ include, among others: our ability to obtain regulatory approvals for our FemBloc product candidate; develop and advance our current FemBloc product candidate and successfully enroll and complete the clinical trial; the ability of our clinical trial to demonstrate safety and effectiveness of our product candidate and other positive results; estimates regarding the total addressable market for our products and product candidate; our ability to commercialize our products and product candidate, our ability to establish, maintain, grow or increase sales and revenues, or the effect of delays in commercializing our products, including FemaSeed; our business model and strategic plans for our products, technologies and business, including our implementation thereof; and those other risks and uncertainties described in the section titled "Risk Factors" in our Annual Report on Form 10-K for the year ended December 31, 2025, and other reports as filed with the SEC. Forward-looking statements contained in this press release are made as of this date, and Femasys undertakes no duty to update such information except as required under applicable law.

Contacts: 
IR@femasys.com
Media@femasys.com


FAQ

AI-generated questions and answers. How Rhea-AI works. Not financial advice.

What were Femasys FEMY’s third-quarter 2026 sales and earnings?

Femasys reported sales of $404,597 and a net loss of $4,564,815 for the quarter ended September 30, 2026. Sales fell 44.5% from $729,394 a year earlier. Net loss widened from $4,194,821, while basic and diluted loss per share narrowed to $0.53 from $2.05.

How much did Femasys raise in its private placement, and what will it fund?

Femasys completed a $30 million private placement to build its U.S. commercial team and fund the FemBloc pivotal trial supporting U.S. approval. Potential total proceeds could reach up to $85 million upon full cash exercise of warrants.

Why did Femasys international FemBloc sales decline in 2026?

Femasys attributes the overall sales decline to international FemBloc order timing, consistent with distributors’ customary bulk-ordering practices. Distributors are using existing inventory for FemBloc post-market studies, with reorders expected after those studies are completed.

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