Medical Device Recalls
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21 to 30 of 81 Results
510(K) Number: K072642 |
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Prep-Tite Post Dental implants | 2 | 08/12/2016 | Biomet 3i, LLC |
Standard Abutment Dental implants | 2 | 08/12/2016 | Biomet 3i, LLC |
Standard Abutment Temporary Screw Dental implants | 2 | 08/12/2016 | Biomet 3i, LLC |
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 |
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