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EBR Systems (EBR) investor relations material
EBR Systems Q4 2025 earnings summary
Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.Executive summary
Achieved FDA approval for leadless left ventricular pacing (WiSE CRT System) in April 2025, enabling U.S. commercial launch targeting heart failure patients unsuitable for traditional CRT.
Commercial rollout began in June 2025, with 30 commercial implants and $1.6 million in revenue by year-end; 18 patients treated in Q4 and 25 in the first two months of the new year.
Strong physician engagement, high demand for training, and a robust pipeline of patients awaiting treatment.
No direct competitors in leadless left ventricular pacing; technology is complementary to major incumbents and is the only FDA-approved leadless LV pacing system.
Established U.S. reimbursement pathways (NTAP and TPT) at a $63,300 contract price, supporting both inpatient and outpatient procedures for three years.
Financial highlights
2025 revenue reached $1.6 million, all from U.S. commercial sales post-FDA approval; Q4 revenue exceeded $900,000 with 18 commercial implants.
Gross profit was $0.5 million with a 30.3% margin, aided by use of previously expensed inventory.
Operating expenses for the quarter were $13.5 million; full-year R&D expense was $23.9 million (down 11.5% YoY), and SG&A was $22.6 million (up 101.1% YoY).
Net loss for 2025 was $48.8 million, up 19.5% from 2024, reflecting increased investment in commercialization and R&D.
Year-end cash, cash equivalents, and marketable securities totaled $54.2 million.
Outlook and guidance
Focus for the year is on ramping sales execution, expanding commercial reach, and preparing for full market release in 2H 2026.
Ongoing post-approval studies (WiSE-UP) and feasibility studies (TLC-AU) to support broader indications and market expansion.
No forward-looking revenue or cash flow guidance provided; refer to analyst consensus for projections.
Substantial doubt exists regarding ability to continue as a going concern without additional capital; plans to seek further funding.
Anticipates further acceleration in patient treatments and hospital contracts.
- Shareholders voted on a reverse stock split and ratification of a prior securities issuance.EBR
EGM 202611 Mar 2026 - Only FDA-approved, fully leadless CRT device, targeting a $5.8bn US market with rapid growth.EBR
Investor presentation9 Mar 2026 - Shareholders to vote on consolidating common shares for future flexibility; ASX CDIs unaffected.EBR
EGM 202621 Jan 2026 - Leadless left ventricular pacing launches with FDA approval, strong adoption, and $5.8B TAM.EBR
44th Annual J.P. Morgan Healthcare Conference15 Jan 2026 - FDA approval, funding, and commercialization plans defined a pivotal year; key proposals were voted.EBR
AGM 202525 Nov 2025 - Q3 2025 revenue surged 201% sequentially, but net loss increased to $12.2 million.EBR
Q3 2025 TU23 Nov 2025 - FDA approval and first U.S. sales of WiSE CRT System mark a pivotal commercialization milestone.EBR
Q2 2025 TU7 Sep 2025 - Leadless CRT device with pivotal trial success targets US$3.6bn market and FDA approval in 2025.EBR
Investor Presentation30 Jun 2025 - Only leadless CRT device with FDA approval expected by April 2025 and $3.6bn market opportunity.EBR
Investor Presentation30 Jun 2025
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