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Lifecare International, Inc.

Country not established

Devices
1

What Lifecare International, Inc. makes

Lifecare International, Inc. manufactures the LIFECARE CPAP-200, which is a continuous positive airway pressure (CPAP) device used for treating sleep apnea.

The company's products are regulated as Class II medical devices and are listed in the FDA 510(k) registry. Lifecare International is based in the US.

AI-generated from registry data, 29 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Lifecare Cpap-200 Ref K933947

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

Frequently asked questions

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

The registry currently lists 1 device for Lifecare International, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Lifecare International, Inc.'s devices?

Among its 1 most recently registered device, Lifecare International, Inc. has devices listed in FDA 510(k) (1 device).

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

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

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

The most recently registered devices listed for Lifecare International, Inc. include LIFECARE CPAP-200.

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