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Heartbeam (BEAT) investor relations material
Heartbeam Oppenheimer 36th Annual Healthcare MedTech & Services Conference summary
Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.Company background and technology
Founded to address the lack of at-home 12-lead ECGs, inspired by a personal loss due to heart attack misrecognition.
Developed a cable-free, synthesized 12-lead ECG platform for real-time, at-home use, with two FDA clearances as of December 2024.
Core IP centers on 3D heart signal collection, enabling both handheld and patch form factors for broad cardiac monitoring applications.
Proprietary technology miniaturizes vectorcardiography, transforming 3D signals into physician-readable 12-lead ECGs.
Market strategy and commercial launch
Initial target market is 1.5 million patients in concierge and preventive cardiology, with pricing set at $500-$1,000 per year per patient on a subscription basis.
High willingness to pay and physician recommendation observed in market research among high-net-worth and concierge practice patients.
Strategy leverages physician practices as sales channels, aiming for deep adoption within executive health and cardiology-focused segments.
Break-even expected within the initial 150,000-patient segment, with plans to scale to broader markets and achieve cash flow positive at 30,000 patients.
Product pipeline and innovation
Platform includes the FDA-cleared handheld device, an on-demand 12-lead patch for ambulatory monitoring, and AI-driven features.
Patch device targets the $2 billion ambulatory cardiac monitoring market, offering both arrhythmia and ischemia detection, with strong physician interest for market adoption.
AI partnerships, notably with Mount Sinai, aim to bring predictive and screening algorithms to home ECGs, expanding beyond symptom-driven use.
Ongoing clinical studies in Europe and Asia support indication expansion for heart attack detection.
- FDA-cleared portable ECG system targets $100M capital raise in expanding cardiac monitoring market.BEAT
Registration Filing13 Mar 2026 - FDA-cleared 12-lead ECG launch, AI partnership, and improved cash position drive growth.BEAT
Q4 202512 Mar 2026 - FDA-cleared, cable-free 12-lead ECG platform targets $40B+ cardiac monitoring market.BEAT
Investor presentation12 Mar 2026 - Shelf registration for $100M supports launch of FDA-cleared portable 12-lead ECG system.BEAT
Registration Filing9 Feb 2026 - Q3 net loss was $5.3M; FDA clearance and commercial launch expected by end of 2025.BEAT
Q3 20253 Feb 2026 - AIMIGO nears FDA clearance as Q2 net loss hits $5M and cash burn raises going concern risk.BEAT
Q2 20241 Feb 2026 - Q3 net loss reached $5.0M; FDA clearance and new funding are critical for future operations.BEAT
Q3 202415 Jan 2026 - FDA clearance and $11.5M funding drive commercial launch of cardiac monitoring technology.BEAT
Q4 202425 Dec 2025 - Annual meeting to elect directors, ratify auditor, and expand equity plan for long-term growth.BEAT
Proxy Filing2 Dec 2025
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