Medical Device Recalls
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1 result found
510(K) Number: K170250 |
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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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| Focalyx Fusion | 2 | 02/03/2026 |
FEI # 3016567400 Focalyx Technologies, LLC. |
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