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HeartBeam to Showcase FDA-Cleared 3D ECG Technology at JP Morgan Healthcare Conference

By Editorial Staff

TL;DR

HeartBeam's FDA-cleared portable ECG technology offers investors early access to a disruptive cardiac care platform ahead of its 2026 commercial launch.

HeartBeam's cable-free system uses 3D ECG signals from five electrodes to synthesize 12-lead ECGs for arrhythmia assessment, with FDA clearance and over 20 patents.

This portable ECG technology enables cardiac monitoring outside medical facilities, improving early detection and access to care for patients with heart conditions.

HeartBeam's innovative cable-free device creates 12-lead ECGs from 3D signals, transforming how cardiac health is monitored beyond traditional clinical settings.

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HeartBeam to Showcase FDA-Cleared 3D ECG Technology at JP Morgan Healthcare Conference

HeartBeam Inc. (NASDAQ: BEAT) announced its participation in the JP Morgan 2026 Annual Healthcare Conference, scheduled for January 12–15, 2026, in San Francisco. CEO Robert Eno and CFO Timothy Cruickshank will be available for off-site meetings with investors and potential commercialization and co-development partners from January 12–14. The company's presence at this prominent industry gathering follows significant regulatory milestones for its cardiac monitoring technology.

The discussions at the conference are expected to center on HeartBeam's recent 510(k) clearance from the U.S. Food and Drug Administration. The clearance pertains to the company's patented, cable-free 12-lead electrocardiogram synthesis software designed for arrhythmia assessment. This regulatory achievement precedes a planned limited commercial launch in the United States during the first quarter of 2026. The company's core innovation is the first cable-free device capable of collecting ECG signals in three dimensions from non-coplanar directions and synthesizing them into a 12-lead ECG. This platform technology is intended for portable use outside traditional medical facilities, aiming to deliver actionable cardiac data directly to physicians for monitoring trends and acute conditions. For more details on the company's technology and mission, visit https://HeartBeam.com.

HeartBeam's 3D ECG technology initially received FDA clearance for arrhythmia assessment in December 2024, with the 12-Lead ECG synthesis software gaining clearance in December 2025. The cleared indications specify that the HeartBeam System is a portable, non-invasive recorder for adult patients in clinical or home settings. It records a 3-lead ECG from five electrodes but does not perform automated cardiac analysis. The accompanying synthesis software creates a visual 12-lead ECG representation from this 3-lead data, intended solely for manual physician assessment of normal sinus rhythm and specific non-life-threatening arrhythmias, including atrial fibrillation and premature complexes. The company emphasizes that the software output is not identical to a standard diagnostic 12-lead ECG and is not intended for assessing conditions like myocardial infarction, ischemia, or life-threatening arrhythmias. The technology is supported by over 20 issued patents. Investors can find the latest updates relating to BEAT in the company's newsroom at https://nnw.fm/BEAT.

The company's scheduled meetings at the JP Morgan conference highlight a critical phase for HeartBeam as it transitions from regulatory approval to market introduction. For business and technology leaders, particularly in the healthcare and medtech sectors, this development signals a tangible advancement in remote patient monitoring and decentralized cardiac care. The ability to generate synthesized 12-lead ECGs outside a clinical setting could potentially reduce healthcare system burdens, enable more proactive management of chronic cardiac conditions, and create new data streams for personalized medicine. The pursuit of commercialization and co-development partners at a premier investor conference underscores the technology's perceived market viability and the competitive landscape for innovative digital health solutions. The planned limited launch in early 2026 will serve as an initial test of clinical adoption and reimbursement pathways for this novel approach to cardiac insight.

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Editorial Staff

Editorial Staff

@editorial-staff

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