Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K063286 |
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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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| BIOMET 3i LTX DENTAL IMPLANTS Model LTX610 (6x10mm) - Plastic tray within Tyvek tray within cardb... | 2 | 03/29/2017 |
FEI # 1038806 Biomet 3i, LLC |
| Cover Screw Dental implants | 2 | 08/12/2016 |
FEI # 1038806 Biomet 3i, LLC |
| Cover Screw, Headless Dental implants | 2 | 08/12/2016 |
FEI # 1038806 Biomet 3i, LLC |
| Implant Cover Screw Dental implants | 2 | 08/12/2016 |
FEI # 1038806 Biomet 3i, LLC |
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