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Envirotents, Inc.

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Devices
1

What Envirotents, Inc. makes

Envirotents, Inc. manufactures the Envirotent (Bed), a Class I medical device designed for patient isolation and environmental control in healthcare settings.

The Envirotent (Bed) is regulated under FDA’s 510(k) pathway as a Class I device and is listed in the FDA’s 510(k) database. 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

  • Envirotent (Bed) Ref K881725

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

Frequently asked questions

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

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

Which registries list Envirotents, Inc.'s devices?

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

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

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

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

The most recently registered devices listed for Envirotents, Inc. include ENVIROTENT (BED).

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