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U.S. Department of Health and Human Services

Medical Device Recalls
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41 to 50 of 81 Results
510(K) Number: K072642
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FDA Recall
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Temporary Healing Retention Cylinder Dental implants 2 08/12/2016 Biomet 3i, LLC
Temporary Hexed Cylinder Dental implants 2 08/12/2016 Biomet 3i, LLC
Temporary Non-Hexed Cylinder Dental implants 2 08/12/2016 Biomet 3i, LLC
Titanium Hexed Uniscrew Dental implants 2 08/12/2016 Biomet 3i, LLC
Titanium Square Uniscrew Dental implants 2 08/12/2016 Biomet 3i, LLC
Conical EP Healing Cap Dental implants 2 08/12/2016 Biomet 3i, LLC
Conical Healing Cap Dental implants 2 08/12/2016 Biomet 3i, LLC
Gingihue 15 Degree Pre-Angled Post Dental implants 2 08/12/2016 Biomet 3i, LLC
Gingihue Post Dental implants 2 08/12/2016 Biomet 3i, LLC
Gold Slotted Screw Dental implants 2 08/12/2016 Biomet 3i, LLC
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