Medical Device Recalls
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1 result found
510(K) Number: K183518 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Preat Nobel Active/Conical-compatible RP Titanium Blank, REF 9000967 | 2 | 03/20/2024 | Preat Corp |
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