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Wrightmedicaltechnologyinc

Country not established

Devices
303

What Wrightmedicaltechnologyinc makes

The company manufactures orthopedic fixation devices, including bone wedges, hammertoe correction systems, and modular hip and knee replacement components such as wingless distal centralizers, acetabular systems, and tibial inserts. Their portfolio also includes preoperative navigation tools for alignment planning in joint surgeries, as well as specialized hardware for bone stabilization and reconstruction.

These devices are regulated under FDA classifications ranging from Class I to Class III, with some falling under the Unclassified (U) category. They are listed via FDA pathways including 510(k) clearances and PMA approvals, reflecting their distribution in the US market.

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

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Frequently asked questions

How many devices does Wrightmedicaltechnologyinc have in the registry?

The registry currently lists 303 devices for Wrightmedicaltechnologyinc. Devices recorded under merged duplicate company entries are counted once.

Which registries list Wrightmedicaltechnologyinc's devices?

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

What risk classes do Wrightmedicaltechnologyinc's devices fall under?

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

What are the newest devices from Wrightmedicaltechnologyinc in the registry?

The most recently registered devices listed for Wrightmedicaltechnologyinc include PROFEMUR Z CLASSIC STEMS, Cannulated Screw System, SMALL BONE WEDGE and BIOFOAM Bone Wedge.

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