Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K950204 |
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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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Product is labeled as LTX XP Miniplant, Dental Implant, Sterile. | 2 | 09/18/2007 | Biomet 3i |
LTX Endosseous Implant 6.0 mm X 11.5 mm and also LTX Endosseous Implant 5.0 mm X 15 mm, Sterile, | 3 | 03/20/2003 | Implant Innovations, Inc. |
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