Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K230316 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Artelon FlexBand Dynamic Matrix Ref: 31057 | 2 | 03/11/2026 |
FEI # 3010673515 International Life Sciences |
| Artelon FLEXBAND TWIST .12 Ref: TW012 3.85x17mm HEX Anchor (Qty 2) 5.0x17mm HEX Anchor (Q... | 2 | 03/11/2026 |
FEI # 3010673515 International Life Sciences |
| Artelon FlexBand Plus Ref: 41054 & 41057 | 2 | 03/11/2026 |
FEI # 3010673515 International Life Sciences |
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