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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 3 of 3 Results
510(K) Number: K230316
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Product Description
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FDA Recall
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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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