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Kormed, Inc.

United StatesFDA 510(k) applicant, unverified

Devices
2

What Kormed, Inc. makes

Kormed, Inc. manufactures biopsy needles and biopsy trays, including Chiba style biopsy needles and bone marrow biopsy trays.

These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry. The company is based in the United States.

AI-generated from registry data, 20 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue2

Newest first, rows 1-2 of 2

Frequently asked questions

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

The registry currently lists 2 devices for Kormed, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Kormed, Inc.'s devices?

Among its 2 most recently registered devices, Kormed, Inc. has devices listed in FDA 510(k) (2 devices).

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

Among its 2 most recently registered devices, the classes recorded for Kormed, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

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

The most recently registered devices listed for Kormed, Inc. include CHIBA STYLE BIOPSY NEEDLE and BONE MARROW BIOPSY TRAY.

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