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LifePath-C · United States

Designed for greater cardiac visibility.

LifePath-C is a wearable 6/12-lead ambulatory ECG monitoring platform being developed to combine continuous monitoring, broader cardiac visibility, and connected review workflows within a single system.

The LifePath-C monitor held between two fingers, showing its size
Status
Under FDA 510(k) review

The challenge

A short clinic ECG captures only a moment.

LifePath-C is being developed as a medical device to support ambulatory cardiac monitoring outside the clinic, providing longitudinal visibility that a brief in-clinic ECG or limited-duration recording may not provide.

Developed as a medical device (IEC 60601 series, ISO 10993, SBOM/threat-modelling posture).

One patient, one year

Seen in clinic

A handful of appointments. Everything between them is unobserved.

Monitored continuously

The same year, with the stretches in between actually covered.

What it’s designed to do

Continuous ambulatory monitoring, built for clinical review.

A broader cardiac picture

A wearable 6/12-lead design is built to capture more of the heart’s electrical activity than 1–2 lead wearables.

Catches what a moment can miss

Continuous ambulatory monitoring is designed for longitudinal capture outside the clinic, not a 10-second clinic ECG or a single-day recording read after the fact.

Structured clinical review

The platform is designed to organize ambulatory recordings and support the clinical review workflow.

Clinician-controlled review

The platform routes recordings for review by the institution’s clinical team. (Elastic Care-operated monitoring is not offered for US deployments.)

Compact and comfortable by design

Engineered to be small and unobtrusive, designed around patient comfort and discreet, everyday wear, without compromising signal quality or clinical fidelity.

Built as a medical device

Developed with attention to safety, usability, cybersecurity, software validation, and risk management.

Regulatory status

LifePath-C is currently under FDA 510(k) review. It is not currently FDA-cleared for commercial distribution in the United States.

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LifePath RPM is cleared by the FDA under 510(k). LifePath-C is currently under FDA 510(k) review and is not available for sale or clinical use in the United States. Elastic Care-managed monitoring services are currently available only in select international markets and may not be available in all jurisdictions. Product availability, indications for use, and detection capabilities vary by jurisdiction and are subject to local clearance or licensing. Information on this site is for general informational purposes and is not medical advice.