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IceCure Medical (ICCM) investor relations material
IceCure Medical Q2 2026 earnings summary
Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.Executive summary
Achieved 45% year-over-year revenue growth to $1.8 million in H1 2026, driven by increased sales of ProSense systems and disposable probes.
U.S. commercial install base grew approximately 70% following FDA clearance for early-stage, low-risk breast cancer, supporting long-term value creation.
Strengthened balance sheet with $12 million in cash and cash equivalents at the end of H1 2026, following $8.5 million in gross proceeds from recent financings.
Advanced the FDA-approved CHOICE Study, integrating it with commercialization to support physician adoption, reimbursement, and broader market adoption.
Commercial and clinical strategies are reinforcing each other, with growing physician adoption generating more real-world evidence.
Financial highlights
Revenue rose 45% year-over-year to $1.8 million in H1 2026, up from $1.25 million or $1.3 million in H1 2025.
Gross profit increased to $548,000 from $349,000, with gross margin improving to 30% from 28% or 30.1% from 26.8%, despite FX headwinds.
Net loss was $8.8 million ($3.17/share) versus $7 million ($3.59/share) in H1 2025.
R&D expenses rose to $4.3 million, sales and marketing to $2.5 million, and G&A to $2.4 million, reflecting investment in growth and FX impacts.
Ended H1 2026 with $12 million in cash and equivalents, up from $8.9 million at year-end 2025.
Outlook and guidance
Expect continued commercial expansion, increased physician adoption, and higher procedure volumes.
CHOICE Study enrollment on track, with first patients expected imminently and a target of 80 patients by March 2027.
Q3 typically sees lower revenue due to seasonality, with Q4 expected to be the strongest quarter.
Ongoing focus on international growth, particularly in Japan and Brazil.
Plans to continue investing in U.S. and international commercial infrastructure, including sales organization and clinical studies.
- First FDA-cleared minimally invasive cryoablation device for breast cancer, driving global growth.ICCM
Investor presentation - Registering 5.5M shares for resale after $5.5M private placement, with dilution risks.ICCM
Registration filing - Q1 2026 revenue up 26% year-over-year, driven by FDA clearance and expanding U.S. adoption.ICCM
Q1 2026 - Up to 16 million shares offered for resale, with proceeds from warrant exercises funding operations.ICCM
Registration filing - Medtech firm seeks $100M for growth, facing legal and market risks.ICCM
Registration filing - Record revenue and regulatory milestones drive rapid adoption and improved financial outlook.ICCM
Q4 2025 - FDA authorizes first minimally invasive cryoablation device for breast cancer in women 70+.ICCM
Investor Update - FDA review of ProSense post-market study advances, with stable Q1 revenue and improved cash flexibility.ICCM
Q1 2025 - North American sales up 42% and margins higher as FDA decision on ProSense approaches.ICCM
Q4 2024
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