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InspireMD Reports Third Quarter 2025 Financial Results

1. InspireMD's CGuard Prime launched in the U.S., generating record revenue. 2. Third quarter revenue rose 39% to $2.5 million, led by CGuard Prime. 3. Net loss of $12.7 million reflects increased operating expenses. 4. Company strengthened leadership with key appointments for strategic growth. 5. CGuard Prime's initial success boosts global demand for InspireMD's products.

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Why Bullish?

InspireMD's significant revenue growth from CGuard Prime reflects market acceptance and potential expansion. Similar cases like other startups turning profitable after strong product launches often lead to stock appreciation.

How important is it?

The successful launch and revenue generation of CGuard Prime are critical milestones impacting investor perception positively. Increase in revenue indicates potential for future sales and investor interest.

Why Short Term?

The immediate effect of revenue growth is likely to reflect in upcoming stock trading. Previous instances where companies see initial success in product launches often lead to short-term stock price increases.

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ISRGMDTABT
Successful initial CGuard Prime U.S. commercial launch drives record quarterly revenue November 04, 2025 07:00 ET  | Source: InspireMD Inc. MIAMI, Nov. 04, 2025 (GLOBE NEWSWIRE) -- InspireMD, Inc. (Nasdaq: NSPR) (“InspireMD” or the “Company”), developer of the CGuard® Prime carotid stent system for the prevention of stroke, today announced financial and operating results for the third quarter and nine months ended September 30, 2025. Recent Business Highlights: Initiated U.S. commercial launch of the CGuard Prime carotid stent systemCompleted over 100 U.S. carotid procedures across leading hospitalsStrengthened leadership team with the appointment of Peter A. Soukas, M.D., as Chief Medical OfficerAppointed Dan Dearen to the Board of Directors as Audit Committee Chairman bringing valuable experience to InspireMD Marvin Slosman, CEO of InspireMD, commented: “Our business demonstrated strong growth across all geographies in the third quarter of 2025. Over the last few months, our team executed our planned U.S. commercial launch of our CGuard Prime carotid stent system, which delivered measurable revenue in our initial commercial quarter in the United States. We continue to see strong demand for our solutions globally, validating our mission as we work to transform the carotid intervention market with a stent first approach." "Further, with the addition of $58 million in gross proceeds to our balance sheet, as announced in July, we are able to continue adding top-tier talent and executing our commercial rollout with intention, purpose, and stamina. We are entering a new era of growth, and I am confident that this team and technology can deliver immense value over the years ahead." Financial Results for the Third Quarter Ended September 30, 2025For the third quarter of 2025, total revenue increased by 39%, to $2.5 million as compared to $1.8 million during the same period of last year. U.S. revenue for the third quarter was $497,000 and international revenue was $2.0 million. This increase was predominantly attributable to CGuard Prime revenue in the U.S., increased penetration of international markets with CGuard, and the favorable impact of changes in foreign exchange rates. Gross profit (revenue less cost of revenues) for the third quarter of 2025 was $864,000 an increase of $450,000 compared to $414,000 for the third quarter of 2024. This increase in gross profit resulted from an increase in revenue and a favorable shift in sales mix towards higher margin revenue from the Company’s U.S. commercial launch, partially offset by higher production variances and training costs. Total operating expenses for the third quarter of 2025 were $13.9 million an increase of 57% compared to $8.9 million for the third quarter of 2024. This increase was primarily due to increases in headcount-related expenses as the Company continued to expand its U.S. personnel, particularly its commercial team, to drive the U.S. commercial launch of CGuard Prime. A second driver of the increase in operating expenses was occupancy and related infrastructure expense related to the establishment of the Company’s U.S. headquarters. Financial income, net for the third quarter of 2025 was $343,000, a decrease of 40% compared to financial income of $572,000 for the third quarter of 2024. This decrease was primarily due to a $118,000 decrease in financial income from investments in marketable securities and money market funds and a $104,000 increase in financial expenses related to changes in exchange rates. Net loss for the third quarter of 2025 was $12.7 million or $0.17 per basic and diluted share, compared to a net loss of $7.9 million or $0.16 per basic and diluted share, for the same period in 2024. As of September 30, 2025, cash and cash equivalents and marketable securities were $63.4 million compared to $34.6 million as of December 31, 2024. Conference Call and Webcast DetailsManagement will host a conference call at 8:30 am ET today, November 4th, to review financial results and provide an update on corporate developments. Following management’s formal remarks, there will be a question-and-answer session. Tuesday, November 4th at 8:30 a.m. ET About InspireMD, Inc.InspireMD seeks to utilize its proprietary MicroNet™ mesh technology to make its products the industry standard for carotid stenting by providing outstanding acute results and durable, stroke-free long-term outcomes. InspireMD’s common stock is quoted on Nasdaq under the ticker symbol NSPR. We routinely post information that may be important to investors on the Company’s website. For more information, please visit www.inspiremd.com. Forward-looking StatementsThis press release contains “forward-looking statements.” Forward-looking statements include, but are not limited to, statements regarding InspireMD or its management team’s expectations, hopes, beliefs, intentions or strategies regarding future events, future financial performance, strategies, expectations, competitive environment and regulation. Such statements may be preceded by the words “intends,” “may,” “will,” “plans,” “expects,” “anticipates,” “projects,” “predicts,” “estimates,” “aims,” “believes,” “hopes,” “potential”, “scheduled” or similar words. Forward-looking statements are not guarantees of future performance, are based on certain assumptions and are subject to various known and unknown risks and uncertainties, many of which are beyond the Company’s control, and cannot be predicted or quantified and consequently, actual results may differ materially from those expressed or implied by such forward-looking statements. Such risks and uncertainties include, without limitation, risks and uncertainties associated with the Company’s history of recurring losses and negative cash flows from operating activities, significant future commitments and the uncertainty regarding the adequacy of its liquidity to pursue its complete business objectives, and substantial doubt regarding its ability to continue as a going concern; the Company’s need to raise additional capital to meet its business requirements in the future and such capital raising may be costly or difficult to obtain and could dilute out stockholders’ ownership interests; the clinical development, commercialization and market acceptance of the Company’s products; whether the clinical trial results for the Company’s products will be predictive of real-world results; an inability to secure and maintain regulatory approvals for the sale of the Company’s products; negative clinical trial results or lengthy product delays in key markets; the Company’s ability to maintain compliance with the Nasdaq listing standards; the Company’s ability to generate significant revenues from its products; estimates of the Company’s expenses, future revenues, capital requirements and its needs for and ability to access sufficient additional financing, including any unexpected costs or delays in the ongoing commercial launch of its products; the Company’s dependence on a single manufacturing facility and its ability to comply with stringent manufacturing quality standards and to increase production as necessary; the risk that the data collected from the Company’s current and planned clinical trials may not be sufficient to demonstrate that its technology is an attractive alternative to other procedures and products; intense competition in the Company’s industry, with competitors having substantially greater financial, technological, research and development, regulatory and clinical, manufacturing, marketing and sales, distribution and personnel resources than it does; entry of new competitors and products and potential technological obsolescence of the Company’s products; inability to carry out research, development and commercialization plans; loss of a key customer or supplier; technical problems with the Company’s research and products and potential product liability claims; product malfunctions; price increases for supplies and components; whether access to the Company’s products is achieved in a commercially viable manner and whether its products receive adequate reimbursement by governmental and other third-party payers; the Company’s efforts to successfully obtain and maintain intellectual property protection covering its products, which may not be successful; adverse federal, state and local government regulation, in the United States, Europe or Israel and other foreign jurisdictions; the fact that the Company conducts business in multiple foreign jurisdictions, exposing it to foreign currency exchange rate fluctuations, logistical and communications challenges, burdens and costs of compliance with foreign laws and political and economic instability in each jurisdiction; security, political and economic instability in the Middle East that could harm the Company’s business, including due to the current security situation in Israel; current or future unfavorable economic and market conditions and adverse developments with respect to financial institutions and associated liquidity risk; and changes in tariffs, trade barriers, price and exchange controls and other regulatory requirements and the impact of such policies on the Company, its customers and suppliers, and the global economic environment. More detailed information about the Company and the risk factors that may affect the realization of forward-looking statements is set forth in the Company’s filings with the Securities and Exchange Commission (SEC), including the Company’s Annual Report on Form 10-K and its Quarterly Reports on Form 10-Q. Investors and security holders are urged to read these documents free of charge on the SEC’s web site at http://www.sec.gov. The Company assumes no obligation to publicly update or revise its forward-looking statements as a result of new information, future events or otherwise. Investor Contacts:Webb CampbellGilmartin Group LLCWebb@gilmartinir.cominvestor-relations@inspiremd.com CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS(1)(Unaudited)(U.S. dollars in thousands, except share and per share data)  Three months endedSeptember 30, Nine months endedSeptember 30,  2025 2024 2025 2024                           Revenues$2,523  $1,810  $5,830  $5,060  Cost of revenues1,659  1,396  4,361  4,023               Gross Profit864  414  1,469  1,037               Operating Expenses:            Research and development3,635  3,915  11,528  9,941  Selling and marketing4,392  1,472  11,314  4,154  General and administrative5,888  3,489  16,157  11,078               Total operating expenses13,915  8,876  38,999  25,173               Loss from operations(13,051) (8,462) (37,530) (24,136)              Financial income, net343  572  505  1,305               Net Loss$(12,708) $(7,890) $(37,025) $(22,831)              Net loss per share – basic anddiluted$(0.17) $(0.16) $(0.64) $(0.58)              WEIGHTED AVERAGE NUMBEROF ORDINARY SHARES USEDIN COMPUTING NET LOSS PERSHARE - basic and diluted73,466,501  48,369,412  58,245,368  39,413,004                CONDENSED CONSOLIDATED BALANCE SHEETS(1)(Unaudited)(U.S. dollars in thousands, except share and per share data) ASSETSSeptember 30,2025 December 31,2024      Current Assets:    Cash and cash equivalents$63,403 $18,916 Marketable securities- 15,721 Accounts receivable:    Trade, net1,961 1,572 Other475 682 Prepaid expenses945 1,060 Inventory3,607 2,570      Total current assets70,391 40,521           Non-current assets:    Long term deposit438 426 Property, plant and equipment, net3,403 2,371 Operating lease right of use assets2,915 2,360 Funds in respect of employee rights upon retirement1,325 1,129      Total non-current assets8,081 6,286      Total assets$78,472 $46,807       CONDENSED CONSOLIDATED BALANCE SHEETS(1)(Unaudited)(U.S. dollars in thousands, except share and per share data) LIABILITIES AND EQUITYSeptember 30,2025 December 31,2024 Current liabilities:      Accounts payable and accruals:      Trade$1,753  $1,254  Other9,063  6,424  Total current liabilities10,816  7,678         Long-term liabilities:      Operating lease liabilities net of current maturities2,367  1,796  Liability for employee rights upon retirement and others1,175  1,247  Total long-term liabilities3,542  3,043         Total liabilities$14,358  $10,721                Equity:      Common stock, par value $0.0001 per share; 150,000,000shares authorized at September 30, 2025, and December 31,2024; 41,919,141 and 26,611,033 shares issued andoutstanding on September 30, 2025, and December 31, 2024,respectively4  3  Preferred C shares, par value $0.0001 per share;1,172,000 shares authorized at September 30, 2025, andDecember 31, 2024; 1,718 shares issued and outstanding atSeptember 30, 2025, and December 31, 2024, respectively*  *  Additional paid-in capital354,641  289,589  Accumulated deficit(290,531) (253,506)        Total equity64,114  36,086         Total liabilities and equity$78,472  $46,807          (1) All September 30, 2025, financial information is derived from the Company’s 2025 unaudited financial statements, as disclosed in the Company’s Quarterly Report on Form 10-Q, filed with the Securities and Exchange Commission on November 10, 2025. All December 31, 2024, financial information is derived from the Company’s 2024 audited financial statements as disclosed in the Company’s Annual Report on Form 10-K, for the twelve months ended December 31, 2024, filed with the Securities and Exchange Commission on March 12, 2025.

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