Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K061319 |
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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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ImplantDirect simply RePlant Implant, size 4.3mmD x 13mmL, 4.3mmD Platform, REF 604313U, Rx, Sterile... | 2 | 10/01/2019 | Implant Direct Sybron Manufacturing, LLC |
REPLANT 5.0mmD ABUTMENT, Part number 6050-52-60 | 2 | 07/05/2018 | Implant Direct Sybron Manufacturing, LLC |
Legacy Full Contour Laboratory Abutment: 3.5mmD Platform/5.5mmD | 2 | 05/22/2017 | Implant Direct Sybron Manufacturing, LLC |
RePlant® Angled Abutment Part Number 6050-52-60 | 2 | 08/02/2016 | Implant Direct Sybron Manufacturing, LLC |
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