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Implant Direct Sybron Manufacturing LLC

10 FDA 510(k) clearances · Recalling firm

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RecordFirmDate
The Drill Stop Kit is the version of the Mini Sterilizable Tray that is used to store, ste recall (Z-2172-2025)Implant Direct Sybron Manufacturing LLC2025-07-25
LEGACY SMARTBASE, NE 3.0D 1MML, REF: 8730-81NE; LEGACY SMARTBASE, NE 3.0D 2MML, REF 8730-8 recall (Z-2037-2023)Implant Direct Sybron Manufacturing LLC2023-06-29
SwishPlus Implant 5.7mmD x 8mmL, SBM 6.5mmD Platform, Part Number 925708 recall (Z-1126-2020)Implant Direct Sybron Manufacturing LLC2020-02-10
Implant Direct, CE 0086, REF: 855710, Legacy 3 Impant, Surface: SBM, Qty:1, Size:5.7mmD x recall (Z-1157-2020)Implant Direct Sybron Manufacturing LLC2020-02-05
Legacy 3 Implant, Size: 4.2mmD x 13mmL, 3.5mmD Platform, REF: 864213 recall (Z-1041-2020)Implant Direct Sybron Manufacturing LLC2020-02-04
Implant Direct, REF: 833708, Legacy 2 Implant, Surface: HA, 3.7mmD x 8mmL, 3.5mmD Platform recall (Z-0364-2020)Implant Direct Sybron Manufacturing, LLC2019-11-12
SwishTapered Implant recall (Z-1112-2017)Implant Direct Sybron Manufacturing, LLC2017-01-28
GoDirect Screw-Retaining Top Part Numbers: 4500-61 recall (Z-0961-2017)Implant Direct Sybron Manufacturing, LLC2017-01-09
RePlant Angled Abutment Part Number 6050-52-60 recall (Z-2320-2016)Implant Direct Sybron Manufacturing, LLC2016-08-02
DGDE, DirectGuide Drill Extender. Instrument for use with dental implants. A manufactured recall (Z-0396-2016)Implant Direct Sybron Manufacturing, LLC2015-12-08

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