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Tosense, Inc.

United StatesFDA applicant, unverified

Devices
2

What Tosense, Inc. makes

Tosense, Inc. manufactures the COVA MONITORING SYSTEM and CoVa Monitoring System 2, which are Class II medical devices.

These devices are listed in the FDA 510(k) registry, and the company is based in the US.

AI-generated from registry data, 30 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue2

Newest first, rows 1-2 of 2

  • Cova Monitoring System Ref K142087

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • CoVa Monitoring System 2 Ref K160899

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

Frequently asked questions

How many devices does Tosense, Inc. have in the registry?

The registry currently lists 2 devices for Tosense, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Tosense, Inc.'s devices?

Among its 2 most recently registered devices, Tosense, Inc. has devices listed in FDA 510(k) (2 devices).

What risk classes do Tosense, Inc.'s devices fall under?

Among its 2 most recently registered devices, the classes recorded for Tosense, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Tosense, Inc. in the registry?

The most recently registered devices listed for Tosense, Inc. include COVA MONITORING SYSTEM and CoVa Monitoring System 2.

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