Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K081396 |
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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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SwishPlus Implant 5.7mmD x 8mmL, SBM 6.5mmD Platform, Part Number 925708 | 2 | 02/10/2020 | Implant Direct Sybron Manufacturing LLC |
SwishPlus Implant Intended for use in support for fixed bridgework. | 2 | 03/22/2018 | Implant Direct Sybron Manufacturing, LLC |
DGDE, DirectGuide Drill Extender. Instrument for use with dental implants. A manufactured device ... | 2 | 12/08/2015 | Implant Direct Sybron Manufacturing, LLC |
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