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Gce Medical Corporation

Country not established

Devices
1

What Gce Medical Corporation makes

Gce Medical Corporation manufactures the Focus Cap, a medical device designed for use in neurostimulation applications, specifically targeting focal epilepsy management through transcranial magnetic stimulation.

The Focus Cap is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.

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

Catalogue1

Newest first, rows 1-1 of 1

  • Focus Cap Ref K171673

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

Frequently asked questions

How many devices does Gce Medical Corporation have in the registry?

The registry currently lists 1 device for Gce Medical Corporation. Devices recorded under merged duplicate company entries are counted once.

Which registries list Gce Medical Corporation's devices?

Among its 1 most recently registered device, Gce Medical Corporation has devices listed in FDA 510(k) (1 device).

What risk classes do Gce Medical Corporation's devices fall under?

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

What are the newest devices from Gce Medical Corporation in the registry?

The most recently registered devices listed for Gce Medical Corporation include Focus Cap.

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