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Pulsenmore (NASDAQ: PLSM) 2025 revenue soars on GE deal as net loss halves

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6-K

Rhea-AI Filing Summary

Pulsenmore Ltd. reported full-year 2025 revenue of $12.5 million, up 374% from 2024, driven mainly by a $9.6 million one-time revenue from a settlement with GE Precision Healthcare that also canceled 15,000-unit orders and ended a component agreement. Excluding this, underlying revenues were far smaller.

The company’s net loss narrowed to $5 million from $10 million, as gross profit rose to $10.5 million and gross margin expanded to about 84% from 37%, despite higher operating expenses of $14.4 million tied to U.S. infrastructure, partnerships, and operations. Pulsenmore ended 2025 with $21.7 million in total liquid assets, including $7 million in cash and cash equivalents. Strategically, it secured FDA clearance for remote-use prenatal ultrasound in the U.S., obtained MDR CE certification in Europe for its early-screening product, and launched initial U.S. commercial programs integrating its home-use ultrasound into clinical workflows.

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Insights

Results show one-time-driven revenue spike, improved loss, and key regulatory wins.

Pulsenmore’s 2025 revenue rose to $12.5 million, but most came from a one-time $9.6 million GE settlement. Core revenues remain modest, so the headline 374% growth over 2024 does not yet reflect a scaled recurring business.

Net loss improved to $5 million from $10 million as gross margin expanded to about 84%, helped by the settlement, while operating expenses increased to $14.4 million due to U.S. build-out and commercialization efforts. Total liquid assets of $21.7 million provide some funding cushion as the company invests.

Strategically, FDA clearance for remote-use prenatal ultrasound in the U.S. and MDR CE certification in Europe create regulatory foundations in major markets. Initial U.S. commercial programs integrating home-use ultrasound into clinical workflows are early but important steps; subsequent filings may clarify how quickly recurring revenues follow these milestones.

Full-year 2025 revenue $12.5 million Year ended December 31, 2025; 374% increase vs 2024
GE settlement revenue $9.6 million One-time revenue contribution in 2025, including ~15,000-unit order cancellation
Net loss 2025 $5 million Year ended December 31, 2025; improved from $10 million in 2024
Gross margin 2025 Approximately 84% Gross profit $10.5 million vs gross margin 37% in 2024
Operating expenses 2025 $14.4 million Year ended December 31, 2025; driven by U.S. scaling and partnerships
Total liquid assets $21.7 million As of December 31, 2025, including $7 million in cash and cash equivalents
Total revenues 2025 (NIS) NIS 40,024 thousand Includes NIS 30,540 thousand from GEHC settlement; USD 12,547 thousand
Total equity $26.048 million Equity as of December 31, 2025 (USD in thousands)
FDA clearance regulatory
"Secured FDA clearance for remote-use prenatal ultrasound in the United States"
FDA clearance is the U.S. Food and Drug Administration’s official permission to market certain medical devices or diagnostic tests after reviewing evidence that they are as safe and effective as similar products already on the market. For investors, it’s like a product passing a required safety inspection — it reduces regulatory uncertainty, speeds commercial rollout, and can directly affect sales prospects, valuation, and partnership opportunities.
Medical Device Regulation (MDR) Conformité Européenne (CE) Certification regulatory
"Received Medical Device Regulation (MDR) Conformité Européenne (CE) Certification for the Pulsenmore Early-Screening"
Settlement Agreement financial
"recognized approximately $9.6 million in one-time revenue in connection with a settlement agreement with GE Precision Healthcare LLC"
A settlement agreement is a legally binding deal where two sides resolve a dispute—often a lawsuit—by agreeing on terms such as payments, actions, or changes in behavior instead of continuing the case to trial. For investors it matters because settlements can create immediate costs, limit future liabilities or risks, and change a company's cash flow, reputation, or ongoing obligations much like paying a negotiated bill to avoid a lengthy, uncertain fight.
De Novo authorization regulatory
"Following our FDA De Novo authorization and Nasdaq listing, we focused on scaling our U.S. infrastructure"
A de novo authorization is a regulatory pathway the U.S. Food and Drug Administration for approving a novel medical device that has no previously cleared “predicate” device and is judged to pose low-to-moderate risk. For investors, it matters because it can allow a company to bring a new product to market faster and with lower cost and regulatory burden than the most stringent approval routes, potentially speeding revenue, improving valuation prospects, and establishing an early competitive foothold.
contract liabilities financial
"Contract liabilities | | 5,133 | | | | 938 |"
Contract liabilities are amounts a company has been paid in advance for goods or services it still owes to customers — think of them like gift cards or prepaid subscriptions the company must fulfill later. For investors, they show promised future work or deliveries that will turn into revenue over time, reveal cash already collected, and help assess whether a firm has a backlog of obligations that could affect future earnings and cash flow.

 

 

 

UNITED STATES

SECURITIES AND EXCHANGE COMMISSION

Washington, D.C. 20549

 

FORM 6-K

 

Report of Foreign Private Issuer Pursuant to Rule 13a-16 or 15d-16

Under the Securities Exchange Act of 1934

 

For the Month of March 2026

 

001-43033

(Commission File Number)

 

PULSENMORE LTD.

(Exact name of Registrant as specified in its charter)

 

8 Omarim St.

Omer 8496500, Israel

(Address of principal executive offices)

 

Indicate by check mark whether the registrant files or will file annual reports under cover Form 20-F or Form 40-F.

 

Form 20-F ☒ Form 40-F ☐

 

 

 

 

 

 

On March 30, 2026, Pulsenmore Ltd. issued a press release entitled “Pulsenmore Announces Full Year 2025 Financial Results and Webcast”. A copy of the press release is attached hereto as Exhibit 99.1 and is incorporated herein by reference.

 

 

 

 

EXHIBIT INDEX

 

Exhibit
No.

  Description
     
99.1   Press Release, dated March 30, 2026.

 

 

 

 

SIGNATURES

 

Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned, thereunto duly authorized.

 

  Pulsenmore Ltd.
     
Date: March 30, 2026 By: /s/ Eran Hirsh
    Eran Hirsh
    Chief Financial Officer

 

 

 

 

 

Exhibit 99.1

 

 

Pulsenmore Announces Full Year 2025 Financial Results and Webcast

 

Management to Host Conference Call and Webcast today at 8:30am ET to Discuss Results and Provide Business Update

 

OMER, Israel, March 30, 2026 /PRNewswire/ – Pulsenmore Ltd. (NASDAQ, TASE: PLSM), a pioneer in home ultrasound technology, today announced financial results for the full year ended December 31, 2025.

 

Full-Year 2025 Financial Highlights

 

Full year revenue of $12.5 million, representing a 374% increase compared to 2024, including a one-time revenue contribution of $9.6 million related to the GE settlement discussed below.
Net loss improved significantly to $5 million, compared to $10 million in 2024.
$21.7 million in total liquid assets (including $7 million in cash and cash equivalents) as of December 31, 2025.
Recognized approximately $9.6 million in one-time revenue in connection with a settlement agreement with GE Precision Healthcare LLC (GEHC), which resolved all outstanding disputes between the parties and concluded all related proceedings. Approximately $2.2 million was recognized as revenue from the cancellation of orders placed by GEHC for 15,000 units pursuant to the Settlement Agreement and the termination of the Component Agreement.

 

Operational Highlights

 

Regulatory milestone – U.S.: Secured FDA clearance for remote-use prenatal ultrasound in the United States, establishing the regulatory foundation for entry into the world’s largest prenatal diagnostics market.
Regulatory milestone – Europe: Received Medical Device Regulation (MDR) Conformité Européenne (CE) Certification for the Pulsenmore Early-Screening (ES) pregnancy product, authorizing commercial distribution across the European Union for single-fetus pregnancies starting at 14 weeks of gestation.
Commercial milestone: Initial U.S. commercial programs validating Pulsenmore ES home-use ultrasound integration with clinical workflows ahead of broader rollout.

 

“2025 was a transformative year for Pulsenmore as we advanced from regulatory achievement to commercial execution,” said Dr. Elazar Sonnenschein, CEO and Founder of Pulsenmore. “Following our FDA De Novo authorization and Nasdaq listing, we focused on scaling our U.S. infrastructure, expanding clinical partnerships, and strengthening our operational capabilities to support long-term growth.

 

We are seeing encouraging validation from providers and health systems who recognize the value of remote, clinician-directed ultrasound as part of modern prenatal care. As we enter 2026, our focus remains on accelerating commercial momentum, increasing utilization, strengthening recurring revenue streams while maintaining disciplined investment. We believe the progress achieved in 2025 positions Pulsenmore to execute on a significant market opportunity in remote prenatal diagnostics.”

 

 

 

 

 

Financial Highlights for Full Year Ended December 31, 2025

 

Revenues for the year ended December 31, 2025 were $12.5 million, compared to approximately $2.6 million for the year ended December 31, 2024. Revenues were primarily contributed by a $9.6 million one-time payment related to the GE settlement.

 

Cost of Revenues was $2.0 million for the year ended December 31, 2025, compared to $1.7 million for the year ended December 31, 2024. The increase primarily reflects higher revenues from both core operations and the one-time settlement, partially offset by improved operational efficiency.

 

Gross Profit was $10.5 million for the year ended December 31, 2025, compared to gross profit of $0.98 million for the year ended December 31, 2024, reflecting a gross margin of approximately 84% in 2025, up from 37% in 2024.

 

Operating expenses were $14.4 million for the year ended December 31, 2025, compared to $12.6 million for the year ended December 31, 2024. The increase was primarily driven by investments in scaling U.S. infrastructure, expanding clinical partnerships, and strengthening operational capabilities.

 

Net loss was $5 million for the year ended December 31, 2025, compared to $10 million for the year ended December 31, 2024, representing a 50% improvement year-over-year.

 

Total liquid assets as of December 31, 2025 was approximately $21.7 million.

 

Webcast Details

 

Pulsenmore will host a webcast to review the full year 2025 results today on March 30th at 8:30 am Eastern Time / 3:30 p.m. Israel Time.

 

Webcast: https://teams.microsoft.com/meet/3845461353556?p=fcIpXc4mErwEAqo3Ir

 

Replay: The meeting will be recorded, and the recording will be made available following the meeting on the Company’s Investor Relations website at: https://pulsenmore.com/investor_relations

 

A copy of Pulsenmore’s annual report on Form 20-F for the year ended December 31, 2025 has been filed with the U.S. Securities and Exchange Commission at https://www.sec.gov/ and posted on Pulsenmore’s investor relations website at https://pulsenmore.com/investor_relations/. Pulsenmore will deliver a hard copy of its annual report, including its complete audited consolidated financial statements, free of charge, to its shareholders upon request at msegal@ms-ir.com.

 

About Pulsenmore

 

Pulsenmore Ltd. is dedicated to revolutionizing maternal health through the development of home-use ultrasound technology that connect mothers and healthcare providers remotely. By leveraging advanced imaging and telemedicine, Pulsenmore makes prenatal care patient-centric, expanding access and improving continuity of care. For more information, visit www.pulsenmore.com

 

 

 

 

 

This press release contains forward-looking statements. In particular, statements using words such as “may,” “seek,” “will,” “consider,” “likely,” “assume,” “estimate,” “expect,” “anticipate,” “intend,” “believe,” “contemplate,” “do not believe,” “aim,” “goal,” “due,” “predict,” “plan,” “project,” “continue,” “potential,” “positioned,” “guidance,” “objective,” “outlook,” “trends,” “future,” “could,” “would,” “should,” “target,” “on track” or their negatives or variations, and similar terminology and words of similar import, generally involve future or forward-looking statements. Such forward-looking statements include, but are not limited to, statements relating to Pulsenmore’s continued commercial momentum, clinician adoption expansion, strengthening its presence in the U.S. market following its Nasdaq listing and FDA De Novo authorization, accelerating commercial momentum, increasing utilization, strengthening recurring revenue streams while maintaining disciplined investment and its belief that the progress achieved in 2025 positions it to execute on a significant market opportunity in remote prenatal diagnostics. Forward-looking statements reflect Pulsenmore’s current views, plans, or expectations with respect to future events or financial performance. They are inherently subject to significant business, economic, competitive, and other risks, uncertainties, and contingencies. Forward-looking statements are based on Pulsenmore’s current expectations and are subject to inherent uncertainties, risks and assumptions that are difficult to predict, including, but not limited to, the following: the Company’s lack of operating history; the Company’s current and future capital requirements and the Company’s belief that its existing cash will be sufficient to fund its operations for more than one year from the date that the financial statements are issued; the Company’s ability to manufacture, market and sell its products and to generate revenues; the Company’s ability to maintain its relationships with key partners and grow relationships with new partners; the Company’s ability to maintain or protect the validity of its U.S. and other patents and other intellectual property; the Company’s ability to launch and penetrate markets in new locations and new market segments; the Company’s ability to retain key executive members and hire additional personnel; the Company’s ability to maintain and expand intellectual property rights; interpretations of current laws and the passages of future laws; the Company’s ability to achieve greater regulatory compliance needed in existing and new markets; the Company’s ability to achieve key performance milestones in its planned operational testing; the Company’s ability to establish adequate sales, marketing and distribution channels; security, political and economic instability in the Middle East that could harm its business; and acceptance of the Company’s business model by investors. Further, certain forward-looking statements are based on assumptions as to future events that may not prove to be accurate. For a more detailed description of the risks and uncertainties affecting the Company, reference is made to the Company’s reports filed from time to time with the SEC, including, but not limited to, the risks, uncertainties and other factors included in the Company’s Annual Report on Form 20-F for the fiscal year ended December 31, 2025 and in subsequent filings with the SEC. The inclusion of forward-looking statements in this or any other communication should not be considered as a representation by Pulsenmore or any other person that current plans or expectations will be achieved. Forward-looking statements speak only as of the date on which they are made, and Pulsenmore undertakes no obligation to publicly update or revise any forward-looking statement, whether as a result of new information, future developments, or otherwise, except as otherwise required by law.

 

Investor Contact:

 

Miri Segal-Scharia

MS-IR LLC

msegal@ms-ir.com

 

 

 

 

 

PULSENMORE LTD.

CONSOLIDATED STATEMENTS OF FINANCIAL POSITION

 

   December 31, 
   2024   2025   2025 
  

NIS in thousands

   USD
in thousands
 
Assets               
CURRENT ASSETS               
Cash and cash equivalents   41,170    21,604    6,773 
Short-term bank deposits   62,853    47,531    14,900 
Restricted deposits   140    140    44 
Trade receivables   3,909    4,144    1,300 
Other receivables   1,237    1,391    436 
Inventory – current portion   23,092    6,593    2,067 
Total current assets   132,401    81,403    25,520 
                
NON-CURRENT ASSETS               
Inventory – non-current portion   -    13,337    4,181 
Right-of-use assets   1,780    1,285    403 
Property and equipment, net   7,645    5,822    1,825 
Total non-current assets   9,425    20,444    6,409 
Total assets   141,826    101,847    31,929 
                
Liabilities and equity               
CURRENT LIABILITIES               
Trade payables   2,359    1,980    621 
Other payables and accruals   3,780    4,407    1,382 
Contract liabilities   5,133    938    294 
Share-based compensation liability   1,458    276    87 
Current maturities of liability for royalties
to the Israel Innovation Authority
   532    1,705    534 
Current maturities of lease liabilities   999    1,023    321 
Total current liabilities   14,261    10,329    3,239 
                
NON-CURRENT LIABILITIES               
Contract liabilities   22,897    -    - 
Share-based compensation liability, net of
current maturities
   164    -    - 
Liability for royalties to the Israel Innovation Authority, net of current
maturities
   6,497    7,886    2,472 
Lease liabilities, net of current maturities   1,120    542    170 
Total non-current liabilities   30,678    8,428    2,642 
Total liabilities   44,939    18,757    5,881 
                
EQUITY               
Ordinary shares   2    2    1 
Share premium   253,205    256,137    80,294 
Capital reserve   10,968    10,092    3,164 
Accumulated deficit   (167,288)   (183,141)   (57,411)
Total equity   96,887    83,090    26,048 
Total liabilities and equity   141,826    101,847    31,929 

 

All share and per share amounts have been retroactively adjusted to reflect a 1-for-8 reverse share split as discussed in Note 1(b)

 

The accompanying notes are an integral part of the consolidated financial statements.

 

 

 

 

 

PULSENMORE LTD.

CONSOLIDATED STATEMENTS OF COMPREHENSIVE LOSS

 

   December 31, 
   2024   2025   2025 
  

NIS in thousands

   USD
in thousands
 
Revenues   9,661    9,484    2,973 
Revenues from settlement agreement
with GEHC (*)
   -    30,540    9,574 
Total revenues   9,661    40,024    12,547 
Cost of revenues   6,084    6,342    1,988 
Gross profit   3,577    33,682    10,559 
                
Research and development expenses, net   20,130    17,350    5,439 
Sales and marketing expenses   10,318    11,815    3,704 
General and administrative expenses   15,344    16,681    5,230 
Operating loss   42,215    12,164    3,814 
                
Financial expenses   540    7,225    2,265 
Financial income   (5,963)   (3,537)   (1,109)
Financial expenses (income), net   (5,423)   3,688    1,156 
                
Loss before income tax   36,792    15,852    4,970 
                
Provision (benefit) for income tax   (56)   1     **  
                
Net loss and comprehensive loss   36,736    15,853    4,970 
                
Loss per ordinary share – basic and
diluted
   5.76    2.46    0.77 

 

* Including an amount of NIS 7.1 million (approximately $2.2 million) was recognized as revenues from the (1) cancellation of orders placed by GEHC to the Company for 15,000 units Pursuant to the Settlement Agreement and (2) due to the termination of the Component Agreement.

 

** Less than $1 thousand

 

 

 

FAQ

How did Pulsenmore (PLSM) perform financially in full-year 2025?

Pulsenmore generated $12.5 million in 2025 revenue, a 374% increase over 2024, mainly from a one-time $9.6 million GE settlement. The company’s net loss narrowed to $5 million from $10 million as gross margin improved sharply.

What was the impact of the GE settlement on Pulsenmore’s 2025 results?

The GE Precision Healthcare settlement contributed about $9.6 million in one-time revenue, including roughly $2.2 million from canceling 15,000-unit orders and terminating a component agreement. This settlement drove most of Pulsenmore’s 2025 revenue growth and boosted gross profit.

How did Pulsenmore’s profitability and margins change in 2025?

Pulsenmore’s net loss improved to $5 million in 2025 from $10 million in 2024. Gross profit increased to $10.5 million, with gross margin rising to about 84% from 37%, reflecting the high-margin GE settlement and better efficiency despite higher operating expenses.

What is Pulsenmore’s cash and liquidity position at year-end 2025?

As of December 31, 2025, Pulsenmore reported $21.7 million in total liquid assets, including $7 million in cash and cash equivalents. This liquidity supports ongoing investments in U.S. infrastructure, clinical partnerships, and commercialization of its home-use prenatal ultrasound products.

What key regulatory milestones did Pulsenmore achieve in 2025?

Pulsenmore secured FDA clearance in the U.S. for remote-use prenatal ultrasound and obtained MDR CE certification in Europe for its early-screening pregnancy product. These milestones authorize commercial distribution across the EU and underpin entry into the U.S. prenatal diagnostics market.

What commercial progress did Pulsenmore make in the U.S. during 2025?

Pulsenmore launched initial U.S. commercial programs that validate integration of its Pulsenmore ES home-use ultrasound with clinical workflows. Management highlighted growing validation from providers and health systems as it focuses on accelerating commercial momentum and strengthening recurring revenue streams.

Where can investors access Pulsenmore’s detailed 2025 financial statements?

Pulsenmore’s Form 20-F for the year ended December 31, 2025, including audited consolidated financial statements, is available on the SEC’s website and the company’s investor relations site. Shareholders can also request a hard copy via the investor relations email provided.

Filing Exhibits & Attachments

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