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Gelb Practice Solutions, Inc.

Country not established

Devices
1

What Gelb Practice Solutions, Inc. makes

Gelb Practice Solutions, Inc. manufactures the airVata™, a medical device designed for respiratory therapy and patient ventilation support.

The company’s portfolio is regulated under FDA Class II devices and is listed via 510(k) clearance. The manufacturer 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

  • airVata™ Ref K240427

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

Frequently asked questions

How many devices does Gelb Practice Solutions, Inc. have in the registry?

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

Which registries list Gelb Practice Solutions, Inc.'s devices?

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

What risk classes do Gelb Practice Solutions, Inc.'s devices fall under?

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

What are the newest devices from Gelb Practice Solutions, Inc. in the registry?

The most recently registered devices listed for Gelb Practice Solutions, Inc. include airVata™.

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