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Gexfix USA, Inc.

Country not established

Devices
1

What Gexfix USA, Inc. makes

Gexfix USA, Inc. manufactures external fixation devices, which are used to stabilize and support fractured bones through external frames attached to the body.

These devices are classified as Class II under FDA regulations and are listed via the 510(k) clearance process. 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

  • External Fixation Ref K052605

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

Frequently asked questions

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

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

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

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

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

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

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

The most recently registered devices listed for Gexfix USA, Inc. include EXTERNAL FIXATION.

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