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U.S. Department of Health and Human Services

Medical Device Recalls

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61 to 70 of 81 Results
510(K) Number: K072642
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Product Description
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FDA Recall
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Certain Standard Abutment Dental implants 2 08/12/2016 Biomet 3i, LLC
Certain Straight Healing Abutment Dental implants 2 08/12/2016 Biomet 3i, LLC
Certain Temporary Hexed Cylinder Dental implants 2 08/12/2016 Biomet 3i, LLC
Certain Temporary Non-Hexed Cylinder Dental implants 2 08/12/2016 Biomet 3i, LLC
Certain Twist Lock TM Coping Dental implants 2 08/12/2016 Biomet 3i, LLC
Conical Abutment Dental implants 2 08/12/2016 Biomet 3i, LLC
Conical Abutment Gold Standard ZR TM Dental implants 2 08/12/2016 Biomet 3i, LLC
Certain EP Healing Abutment 4.1mm(D) x 5mm(P) x 2mm(H) Item: ITHA52 Dental implants 2 08/12/2016 Biomet 3i, LLC
Bellatek Encode Healing Abutment Dental implants 2 08/12/2016 Biomet 3i, LLC
Certain Bellatek Encode Healing Abutment Dental implants 2 08/12/2016 Biomet 3i, LLC
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