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U.S. Department of Health and Human Services

Medical Device Recalls

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51 to 60 of 81 Results
510(K) Number: K072642
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Product Description
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FDA Recall
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Gold -Tite Hexed Retaining Screw Dental implants 2 08/12/2016 Biomet 3i, LLC
Healing Abutment Dental implants 2 08/12/2016 Biomet 3i, LLC
IOL Abutment and Screw Dental implants 2 08/12/2016 Biomet 3i, LLC
IOL Distal Extension Dental implants 2 08/12/2016 Biomet 3i, LLC
IOL Healing Cap Dental implants 2 08/12/2016 Biomet 3i, LLC
IOL Titanium Temporary Cylinder Dental implants 2 08/12/2016 Biomet 3i, LLC
Certain IOL Abutment Dental implants 2 08/12/2016 Biomet 3i, LLC
Certain Preformance 15 degrees Pre-Angled Post Dental implants 2 08/12/2016 Biomet 3i, LLC
Certain Preformance Post Dental implants 2 08/12/2016 Biomet 3i, LLC
Certain Provide Abutment Dental implants 2 08/12/2016 Biomet 3i, LLC
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