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Kirschner Medical Corp.

Also registered as Kirkschner Medical Corp.

United StatesFDA applicant, unverified

Devices
77

What Kirschner Medical Corp. makes

Kirschner Medical Corp. manufactures orthopedic implants and spinal instrumentation, including hip and knee prostheses (such as the Austin Moore, Dimension Total Hip, and Kirschner Modular TCIV Total Knee), shoulder systems (e.g., the Kirschner Modular II-C Total Shoulder), and resurfacing prosthetics (Neer-III Glenoid Resurfacing). The company also produces orthopedic fixation devices like wire, Steinman pins, and compression systems, alongside dosimetric radiation release tools and segmental spinal instrumentation for surgical stabilization.

The company’s portfolio includes devices classified as Class I, Class II, and Class III under FDA regulations, with many cleared via the 510(k) pathway. Products are listed in the FDA’s 510(k) database, reflecting their regulatory authorization status. The manufacturer is based in the United States.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue77

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Frequently asked questions

How many devices does Kirschner Medical Corp. have in the registry?

The registry currently lists 77 devices for Kirschner Medical Corp.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Kirschner Medical Corp.'s devices?

Among its 50 most recently registered devices, Kirschner Medical Corp. has devices listed in FDA 510(k) (50 devices).

What risk classes do Kirschner Medical Corp.'s devices fall under?

Among its 50 most recently registered devices, the classes recorded for Kirschner Medical Corp.'s devices are Class II and Class III. Each device page shows its own class and authorisation.

What are the newest devices from Kirschner Medical Corp. in the registry?

The most recently registered devices listed for Kirschner Medical Corp. include DOSIMETRIC RELEASE OF GAMMA RADIATION, AUSTIN MOORE HIP PROSTHESIS, DIMENSION TOTAL HIP PROSTHESIS and COMPRESSION SYSTEM.

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