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Chronisense Medical, Ltd.

IsraelFDA applicant, unverified

Devices
1

What Chronisense Medical, Ltd. makes

Chronisense Medical, Ltd. manufactures the Polso Watch, a wearable device designed for continuous, non-invasive monitoring of cardiac and vascular health metrics, including pulse and blood pressure trends.

The Polso Watch is classified as a Class II medical device in the U.S. and is listed under the FDA’s 510(k) pathway. The company is based in the United States.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Polso Watch Ref K220351

    Active Regimes: 510(k) Registry: 510(k) Class:II

Frequently asked questions

How many devices does Chronisense Medical, Ltd. have in the registry?

The registry currently lists 1 device for Chronisense Medical, Ltd.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Chronisense Medical, Ltd.'s devices?

Among its 1 most recently registered device, Chronisense Medical, Ltd. has devices listed in FDA 510(k) (1 device).

What risk classes do Chronisense Medical, Ltd.'s devices fall under?

Among its 1 most recently registered device, the classes recorded for Chronisense Medical, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Chronisense Medical, Ltd. in the registry?

The most recently registered devices listed for Chronisense Medical, Ltd. include Polso Watch.

Generated automatically from registry data and not verified by a human reviewer.