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International Medical Device Partners, Inc.

Country not established

Devices
1

What International Medical Device Partners, Inc. makes

International Medical Device Partners, Inc. manufactures the Guarded Needle 2000, a device designed to reduce needle-stick injuries during medical procedures by providing a protective barrier around the needle.

The Guarded Needle 2000 is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. 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

  • Guarded Needle 2000 Ref K003406

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

Frequently asked questions

How many devices does International Medical Device Partners, Inc. have in the registry?

The registry currently lists 1 device for International Medical Device Partners, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list International Medical Device Partners, Inc.'s devices?

Among its 1 most recently registered device, International Medical Device Partners, Inc. has devices listed in FDA 510(k) (1 device).

What risk classes do International Medical Device Partners, Inc.'s devices fall under?

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

What are the newest devices from International Medical Device Partners, Inc. in the registry?

The most recently registered devices listed for International Medical Device Partners, Inc. include GUARDED NEEDLE 2000.

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