Fx Shoulder USA, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 11
What Fx Shoulder USA, Inc. makes
Fx Shoulder USA, Inc. makes shoulder prosthesis components including humeral cups, glenospheres, baseplates, and complete shoulder systems such as the Easytech® Anatomical Shoulder System, Humeris® 135 Shoulder System, and FX V135 Shoulder Prosthesis, with specific products like the Humelock TiN Coated Glenosphere and TiN Coated Humeral Head.
The company's 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.
Catalogue
Search and filter all 11 devicesFrequently asked questions
How many devices does Fx Shoulder USA, Inc. have in the registry?
The registry currently lists 11 devices for Fx Shoulder USA, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Fx Shoulder USA, Inc.'s devices?
Among its 11 most recently registered devices, Fx Shoulder USA, Inc. has devices listed in FDA 510(k) (11 devices).
What risk classes do Fx Shoulder USA, Inc.'s devices fall under?
Among its 11 most recently registered devices, the classes recorded for Fx Shoulder USA, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Fx Shoulder USA, Inc. in the registry?
The most recently registered devices listed for Fx Shoulder USA, Inc. include Humeral Cup Stability & Humeral Cup 135/145o Stability, Full Wedge Lateralized and Augmented Baseplates, 32mm Glenosphere and Humeral Cup and Easytech® Anatomical Shoulder System.