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Wright Medical Technology, Inc. (Stryker)

Also registered as Wright Medical Technology, Inc. (Stryker Corporation)

United StatesFDA applicant, unverified

Devices
5

What Wright Medical Technology, Inc. (Stryker) makes

Wright Medical Technology, Inc. designs and manufactures the Prophecy Surgical Planning System, a software-based tool for pre-operative ankle surgery planning, and the Incompass Total Ankle System, a prosthetic replacement for ankle joints.

The company’s portfolio is regulated under FDA Class II devices, with products authorised via the 510(k) pathway. The devices are listed in the FDA’s 510(k) registry. The manufacturer is based in the United States.

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

Catalogue5

Newest first, rows 1-5 of 5

Frequently asked questions

How many devices does Wright Medical Technology, Inc. (Stryker) have in the registry?

The registry currently lists 5 devices for Wright Medical Technology, Inc. (Stryker). Devices recorded under merged duplicate company entries are counted once.

Which registries list Wright Medical Technology, Inc. (Stryker)'s devices?

Among its 5 most recently registered devices, Wright Medical Technology, Inc. (Stryker) has devices listed in FDA 510(k) (5 devices).

What risk classes do Wright Medical Technology, Inc. (Stryker)'s devices fall under?

Among its 5 most recently registered devices, the classes recorded for Wright Medical Technology, Inc. (Stryker)'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Wright Medical Technology, Inc. (Stryker) in the registry?

The most recently registered devices listed for Wright Medical Technology, Inc. (Stryker) include Prophecy Incompass Surgical Planning System, Synchfix EVT, Allomatrix (Allomatrix Injectable Putty; Allomatrix C; Allomatrix DR; Allomatrix Custom) and Prophecy Surgical Planning System.

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