IceCure Medical (ICCM) Q1 2025 earnings summary
Event summary combining transcript, slides, and related documents.
Q1 2025 earnings summary
17 Mar, 2026Executive summary
Submitted a post-market study plan to the FDA for ProSense cryoablation in early-stage breast cancer for women aged 70+, with optimism for marketing authorization and strong interest from breast surgeons and interventional radiologists.
Achieved continued growth in ProSense systems and disposable probe sales in North America, offsetting declines in Asia, with Europe also showing strong growth.
Largest shareholder provided a $2 million unsecured bridge loan, enhancing financial flexibility and reflecting confidence in the business outlook.
Multiple upcoming milestones in 2025, including regulatory filings in Japan and Israel, and new third-party data publications.
ProSense and ICE3 study received notable recognition at major medical conferences, including ASBRS 2025.
Financial highlights
Q1 2025 revenue was $725,000, down from $743,000 in Q1 2024, driven by growth in North America and Europe but offset by declines in Asia.
Gross profit was $218,000 (gross margin 30%), compared to $269,000 (gross margin 36%) in Q1 2024.
Operating expenses were $3.88 million, slightly down from $3.92 million year-over-year.
Net loss was $3.59 million ($0.06 per share), compared to $3.61 million ($0.08 per share) in Q1 2024.
Cash and equivalents were $6.04 million as of March 31, 2025, and $6.2 million as of May 27, 2025, including the bridge loan.
Outlook and guidance
No material change in revenues expected before FDA marketing authorization decision; revenues and gross profits expected to remain variable as commercial scale builds.
Post-market study will enroll 400 patients across at least 25 sites, with recruitment expected within three years.
Anticipate regulatory filings and potential approvals in Japan (H2 2025) and Israel, plus new third-party data releases.
U.S. sales team expansion planned following marketing authorization.
Latest events from IceCure Medical
- First FDA-cleared minimally invasive cryoablation device for breast cancer, driving global growth.ICCM
Investor presentation14 Jul 2026 - FDA authorizes first minimally invasive cryoablation device for breast cancer in women 70+.ICCM
Investor Update9 Jul 2026 - North American sales up 42% and margins higher as FDA decision on ProSense approaches.ICCM
Q4 20248 Jul 2026 - Q1 2026 revenue up 26% year-over-year, driven by FDA clearance and expanding U.S. adoption.ICCM
Q1 20268 Jul 2026 - Registering 5.5M shares for resale after $5.5M private placement, with dilution risks.ICCM
Registration filing25 Jun 2026 - Up to 16 million shares offered for resale, with proceeds from warrant exercises funding operations.ICCM
Registration filing1 Apr 2026 - Medtech firm seeks $100M for growth, facing legal and market risks.ICCM
Registration filing20 Mar 2026 - Record revenue and regulatory milestones drive rapid adoption and improved financial outlook.ICCM
Q4 202517 Mar 2026 - First FDA-cleared minimally invasive cryoablation for breast cancer, poised for rapid global growth.ICCM
Company presentation16 Mar 2026