Medical Device Recalls
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81 to 81 of 81 Results
510(K) Number: K072642 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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BIOMET 3i Certain MicroMiniplant Straight Healing Abutment, Model/Item Number: ISMHA32, 3.4mm(D) X 0... | 3 | 03/28/2008 | Biomet 3i, Inc. |
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