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Gus Company, Inc.

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Devices
1

What Gus Company, Inc. makes

Gus Company, Inc. manufactures the GUS TRAC C-303, a Class II medical device designed for tracking or monitoring applications in clinical or procedural settings.

The GUS TRAC C-303 is regulated under the FDA’s 510(k) pathway as a Class II device and is listed in the FDA’s 510(k) database. The company is based in the United States.

AI-generated from registry data, 1 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Gus Trac C-303 Ref K872780

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

Frequently asked questions

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

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

Which registries list Gus Company, Inc.'s devices?

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

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

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

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

The most recently registered devices listed for Gus Company, Inc. include GUS TRAC C-303.

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