Fx Shoulder USA, Inc.
11 FDA 510(k) clearances · Manufacturer
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| Record | Firm | Date |
|---|---|---|
| Full Wedge Lateralized and Augmented Baseplates (K240278) | Fx Shoulder USA, Inc. | 2024-05-15 |
| FX V135(TM) Shoulder Prosthesis (K223801) | Fx Shoulder USA, Inc. | 2023-06-05 |
| Humeris® 135 Shoulder System (K222936) | Fx Shoulder USA, Inc. | 2022-11-07 |
| FX V135 Shoulder Prosthesis (K213117) | Fx Shoulder USA, Inc. | 2022-06-07 |
| Lateralized and Augmented Baseplates (K210790) | Fx Shoulder USA, Inc. | 2021-08-25 |
| Easytech® Anatomical Shoulder System (K201391) | Fx Shoulder USA, Inc. | 2021-02-16 |
| TiN Coated Humeral Head (K191698) | Fx Shoulder USA, Inc. | 2020-07-16 |
| Humelock TiN Coated Glenosphere (K191146) | Fx Shoulder USA, Inc. | 2020-07-15 |
| Humeral Cup Stability & Humeral Cup 135/145o Stability (K193394) | Fx Shoulder USA, Inc. | 2020-04-29 |
| Glenoid Baseplate with Screw (K192799) | Fx Shoulder USA, Inc. | 2020-02-21 |
| 32mm Glenosphere and Humeral Cup (K192206) | Fx Shoulder USA, Inc. | 2019-10-08 |
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Every clearance here is in the API, with alerts when new ones post.