Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K102209 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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CERTAIN(R) BELLATEK(R) TIN ABUTMENT 3.4MM, Item Number IEDAN3 - Product Usage: BIOMET3i Restorative ... | 2 | 08/02/2019 | Biomet 3i, LLC |
CERTAIN(R) BELLATEK(R) TITANIUM ABUTMENT 3.4MM, Item Number IEDAT3 - Product Usage: BIOMET3i Restora... | 2 | 08/02/2019 | Biomet 3i, LLC |
CERTAIN(R) BELLATEK(R) TITANIUM ABUTMENT 3.4MM, Item Number ILDAT3 - Product Usage:BIOMET3i Restorat... | 2 | 08/02/2019 | Biomet 3i, LLC |
CERTAIN(R) BELLATEK(R) TIN ABUTMENT 3.4MM, Item Number ILDAN3 - Product Usage: BIOMET3i Restorative ... | 2 | 08/02/2019 | Biomet 3i, LLC |
CERTAIN(R) BELLATEK(R) TITANIUM ABUTMENT 3.4MM, Item Number IIAT3 - Product Usage: BIOMET3i Restora... | 2 | 08/02/2019 | Biomet 3i, LLC |
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