Fluid overload sends heart failure and cirrhosis patients back to hospital. We are building a way to see it coming.

Heart failure drives over 1.2 million U.S. hospital admissions a year, at a cost of tens of billions of dollars. Most begin with the same event: fluid overload.

We are building a wearable monitoring platform that measures fluid directly, so millions of heart and liver patients can stay healthy, and stay home.

A woman in her sixties sits on the edge of her bed at home, one foot resting on a low stool, a slim band around her ankle.

Where we are

Nov 2025Peer-reviewed systematic review of wearable bioimpedance in heart failure published
Mar 2026Incorporated as a federal corporation
Mar 2026Controlled quality management system in place
2026Working research prototype
2026Electrical safety file aligned to IEC 60601-1
Q3 2026Bilingual clinical protocol finalized
Q3 2026Investigational Testing Authorization process started
Q3 2026Hospital ethics review process started at CISSS des Laurentides
Q3 2026Accepted into Life Sciences Central (MaRS, OBIO, TIAP)

Roughly CAD $15,000 of founder capital bought all of this. We will reach first-in-patient data for under CAD $35,000 all-in, and will not open a pre-seed round until that data exists.

How we go to market

We sell first to the people who know the disease. A specialist practice gets patients with daily support who see and own their fluid data, a stronger clinic relationship, and recurring revenue under existing billing codes. One clinic at a time, that builds product intelligence and health-system champions before we approach a hospital or insurer.

Read the approach

Follow the work

We publish a one-page update each quarter and report milestones met and missed. No claims ahead of data.

Join the quarterly update