Skip to content

Therozone USA, Inc.

Country not established

Devices
1

What Therozone USA, Inc. makes

Therozone USA, Inc. manufactures the T-8000 THEROZONE UNIT, which is a Class I medical device.

The company is based in the US and its device is listed in the FDA 510(k) registry.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • T-8000 Therozone Unit Ref K141504

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

Frequently asked questions

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

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

Which registries list Therozone USA, Inc.'s devices?

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

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

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

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

The most recently registered devices listed for Therozone USA, Inc. include T-8000 THEROZONE UNIT.

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