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Thm Biomedical, Inc.

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Devices
1

What Thm Biomedical, Inc. makes

Thm Biomedical, Inc. manufactures the OSMED EPI-GUIDE, which is a medical device used for surgical guidance.

The company is based in the United States, and its product is classified as a Class II medical device that 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

  • Osmed Epi-Guide Ref K940643

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

Frequently asked questions

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

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

Which registries list Thm Biomedical, Inc.'s devices?

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

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

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

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

The most recently registered devices listed for Thm Biomedical, Inc. include OSMED EPI-GUIDE.

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