Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K972444 |
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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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Certain Gingihue TM 15 degree Angled Post Dental implants | 2 | 08/12/2016 | Biomet 3i, LLC |
Certain Titanium Large Hexed Screw Dental implants | 2 | 08/12/2016 | Biomet 3i, LLC |
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