Medical Device Recalls
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51 to 60 of 81 Results
510(K) Number: K072642 |
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
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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