Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K243578 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| BEAR Implant (Bridge-Enhanced ACL Restoration); Model/Catalog: 1000; | 2 | 11/07/2025 | Miach Orthopaedics |
| BEAR Implant. Model Number: 1000. | 2 | 01/29/2026 | Miach Orthopaedics |
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