United Orthopedic Corporation
4 FDA 510(k) clearances · Recalling firm
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| Record | Firm | Date |
|---|---|---|
| USTAR II Hip System Press-Fit Curved Stem, RHS Ti Plasma Spray for the following reference recall (Z-1215-2024) | United Orthopedic Corporation | 2024-02-29 |
| USTAR II Knee System Cemented curved stem, RHS, Non Coated for the following reference num recall (Z-1216-2024) | United Orthopedic Corporation | 2024-02-29 |
| USTAR II Knee System : Cemented Curved Stem, RHS Ti Plasma Spray, Reference Numbers: REF: recall (Z-1217-2024) | United Orthopedic Corporation | 2024-02-29 |
| UOC Femoral Driver, Product number PE 93045101, orthopedic manual surgical instrument/acce recall (Z-1692-2017) | United Orthopedic Corporation | 2017-03-01 |
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Every clearance here is in the API, with alerts when new ones post.