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Medifloat, Inc.

Country not established

Devices
1

What Medifloat, Inc. makes

Medifloat, Inc. makes the MEDAIR EXCEL 2000, a medical device used for respiratory support or airway management, based on its classification and naming convention.

The MEDAIR EXCEL 2000 is classified as a Class II device and is listed in the FDA 510(k) registry. The company is based in the United States.

AI-generated from registry data, 20 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Medair Excel 2000 Ref K942920

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

Frequently asked questions

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

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

Which registries list Medifloat, Inc.'s devices?

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

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

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

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

The most recently registered devices listed for Medifloat, Inc. include MEDAIR EXCEL 2000.

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