Medical Device Recalls
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1 result found
510(K) Number: K242686 |
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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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| Straumann n!ce PMMA Full-arch Restoration. Screw-retained Bridge. Article 010.0304. Endosseous De... | 2 | 04/29/2026 |
FEI # 1000121052 Straumann USA LLC |
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