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
|
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Locator Light Retention Replacement Males 4pk Dental implants | 2 | 08/12/2016 | Biomet 3i, LLC |
Locator Abutment Dental implants | 2 | 08/12/2016 | Biomet 3i, LLC |
Locator Extended Range 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 Extra Light Retention Males 4pk Dental implants | 2 | 08/12/2016 | Biomet 3i, LLC |
Certain Locator Abutment Dental implants | 2 | 08/12/2016 | Biomet 3i, LLC |
Locator Replacement Housing Dental implants | 2 | 08/12/2016 | Biomet 3i, LLC |
Locator Replacement Housing Kit Dental implants | 2 | 08/12/2016 | Biomet 3i, LLC |
Locator Replacement Males 4pk Dental implants | 2 | 08/12/2016 | Biomet 3i, LLC |
BIOMET 3i LOCATOR ABUTMENT, Catalog/Item Number: LOA002, 2.0mm, BioMet 3i, Palm Beach, FL. | 3 | 06/25/2015 | Biomet 3i, Inc. |
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