Medical Device Recalls
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1 to 10 of 11 Results
510(K) Number: K012911 |
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Locator Replacement Males 4pk Dental implants | 2 | 08/12/2016 | Biomet 3i, LLC |
Locator Replacement Housing Kit Dental implants | 2 | 08/12/2016 | Biomet 3i, LLC |
Locator Replacement Housing Dental implants | 2 | 08/12/2016 | Biomet 3i, LLC |
Locator Light Retention Replacement Males 4pk Dental implants | 2 | 08/12/2016 | Biomet 3i, LLC |
Locator Extra Light Retention Males 4pk Dental implants | 2 | 08/12/2016 | Biomet 3i, LLC |
Locator Extra Light Angled Replacement Males 4pk Dental implants | 2 | 08/12/2016 | Biomet 3i, LLC |
Locator Extended Range Males 4pk Dental implants | 2 | 08/12/2016 | Biomet 3i, LLC |
Locator Abutment Dental implants | 2 | 08/12/2016 | Biomet 3i, LLC |
LOCATOR Restorative Abutment, ILOA002, LOT 877423, Certain LOCATOR ABUTMENT, 4.1 mm(D) X 2mm(H), STE... | 2 | 02/22/2010 | Biomet 3i, LLC |
Certain Locator Abutment Dental implants | 2 | 08/12/2016 | Biomet 3i, LLC |
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