Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K891613 |
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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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| O-Ring Abutment 4.1mm(D) x 2mm(H) Item: OSO20 Dental implants | 2 | 08/12/2016 |
FEI # 1038806 Biomet 3i, LLC |
| O-Ring Abutment 4.1mm(D) x 4mm(H) Item: OSO40 Dental implants | 2 | 08/12/2016 |
FEI # 1038806 Biomet 3i, LLC |
| DAL-RO Threaded Female Dental implants | 2 | 08/12/2016 |
FEI # 1038806 Biomet 3i, LLC |
| DAL-RO Housing, Female Assembly Dental implants | 2 | 08/12/2016 |
FEI # 1038806 Biomet 3i, LLC |
| DAL-RO Abutment Dental implants | 2 | 08/12/2016 |
FEI # 1038806 Biomet 3i, LLC |
| O-Ring Abutment 4.1mm(D) x 6mm(H) Item: OSO60 Dental implants | 2 | 08/12/2016 |
FEI # 1038806 Biomet 3i, LLC |
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