54 results
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67ms
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Sources: EU EUDAMED, US FDA
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Status: Terminated
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ImplantDirect Legacy 3 Implant, REF 855216, SBM implant assembly, 2mmD x 16mmL, 4.5mmD platform, Rx, Sterile. The mislabeled model/part number on the vial cap is 835216. The responsible firm on the label is Implant Direct Sybron Manufacturing LLC, Thousand Oaks, CA. - Product Usage:Implant Direct Sybron Manufacturing LLC s dental implant product line consists of one-piece and two-piece implants for one-stage or two-stage surgical procedures. These implants are intended for use in partially and fully edentulous upper and lower jaws in support of single or multiple-unit restorations and terminal or intermediate abutment support for fixed bridgework.
FDA Enforcement
Class II
·Terminated·Implant Direct Sybron Manufacturing, LLC·October 9, 2019
Implant Direct Legacy Implant Closed-Tray Transfer-Concave Profile, 3.5mmD Platform. Dental implant component, used temporarily during impressions for the prosthetic procedure.
FDA Recall
Terminated
·Implant Direct Sybron Manufacturing, LLC·Product code NDP·May 29, 2018
REPLANT 5.0mmD ABUTMENT, Part number 6050-52-60
FDA Recall
Terminated
·Implant Direct Sybron Manufacturing, LLC·Product code DZE·May 18, 2018
The Spectra-System Dental Implant 2008 system is comprised of dental implant fixtures and prosthetic devices that compose a two-piece implant system. GoDirect Implants Part Number: 423011, 423013, 424708, 424710, 424713,433010,433710
FDA Recall
Terminated
·Implant Direct Sybron Manufacturing, LLC·Product code DZE·March 4, 2016
ImplantDirect simply RePlant Implant, size 4.3mmD x 13mmL, 4.3mmD Platform, REF 604313U, Rx, Sterile. The firm name on the label is Implant Direct Sybron Manufacturing LLC, Thousand Oaks, CA.
FDA Enforcement
Class II
·Terminated·Implant Direct Sybron Manufacturing, LLC·October 9, 2019
ImplantDirect Legacy(TM) 3 Implant, 13MM L, REF 864713 This Legacy implant is a two-piece implant for one-stage or two-stage surgical procedures. These implants are intended for use in partially and fully edentulous upper and lower jaws in support of single or multiple-unit restorations and terminal or intermediate abutment support for fixed bridgework.
FDA Recall
Terminated
·Implant Direct Sybron Manufacturing, LLC·Product code DZE·October 10, 2017
Implant Direct, REF: 833708, Legacy 2 Implant, Surface: HA, 3.7mmD x 8mmL, 3.5mmD Platform, RxOnly, Sterile R, Made in USA Dental Implants
FDA Recall
Terminated
·Implant Direct Sybron Manufacturing, LLC·Product code DZE·August 9, 2019
ImplantDirect Legacy 3 Implant, REF 855216, SBM implant assembly, 2mmD x 16mmL, 4.5mmD platform, Rx, Sterile. The mislabeled model/part number on the vial cap is 835216. The responsible firm on the label is Implant Direct Sybron Manufacturing LLC, Thousand Oaks, CA. - Product Usage:Implant Direct Sybron Manufacturing LLC s dental implant product line consists of one-piece and two-piece implants for one-stage or two-stage surgical procedures. These implants are intended for use in partially and fully edentulous upper and lower jaws in support of single or multiple-unit restorations and terminal or intermediate abutment support for fixed bridgework.
FDA Recall
Terminated
·Implant Direct Sybron Manufacturing, LLC·Product code DZE·August 8, 2018
ImplantDirect simply RePlant Implant, size 4.3mmD x 13mmL, 4.3mmD Platform, REF 604313U, Rx, Sterile. The firm name on the label is Implant Direct Sybron Manufacturing LLC, Thousand Oaks, CA.
FDA Recall
Terminated
·Implant Direct Sybron Manufacturing, LLC·Product code DZE·August 7, 2018
The Spectra-System Dental Implant 2008 system is comprised of dental implant fixtures and prosthetic devices that compose a two-piece implant system. GoDirect Implants Part Number: 423011, 423013, 424708, 424710, 424713,433010,433710
FDA Enforcement
Class II
·Terminated·Implant Direct Sybron Manufacturing, LLC·April 6, 2016
RePlant Angled Abutment Part Number 6050-52-60
FDA Recall
Terminated
·Implant Direct Sybron Manufacturing, LLC·Product code DZE·July 5, 2016
Legacy Full Contour Laboratory Abutment: 3.5mmD Platform/5.5mmD
FDA Recall
Terminated
·Implant Direct Sybron Manufacturing, LLC·Product code DZE·May 2, 2017
DGDE, DirectGuide Drill Extender. Instrument for use with dental implants. A manufactured device that adds a 6mm extension for a 25mm and 28mm tissue height capability suitable for individual patient needs. The thru hole in the DGDE allows existing surgical drills to be inserted and locked in place.
FDA Enforcement
Class II
·Terminated·Implant Direct Sybron Manufacturing, LLC·December 16, 2015
Implant Direct Scan Adapter Assembly Replant platform for the following part numbers: 6035-09PT-M (3.5mmD)/UDI : 10841307123934,;6043-09PT-M (4.3mmD)/UDI : 10841307123941; and 6050-09PT-M (5.00mmD)/ UDI: 10841307123958
FDA Recall
Terminated
·Implant Direct Sybron Manufacturing, LLC·Product code NDP·September 6, 2018
DGDE, DirectGuide Drill Extender. Instrument for use with dental implants. A manufactured device that adds a 6mm extension for a 25mm and 28mm tissue height capability suitable for individual patient needs. The thru hole in the DGDE allows existing surgical drills to be inserted and locked in place.
FDA Recall
Terminated
·Implant Direct Sybron Manufacturing, LLC·Product code NHA·October 28, 2015
Implant Direct, CE 0086, REF: 855710, Legacy 3 Impant, Surface: SBM, Qty:1, Size:5.7mmD x 10mmL, 5.7mmD Platform, RxOnly, Sterile R,
FDA Recall
Terminated
·Implant Direct Sybron Manufacturing LLC·Product code DZE·October 11, 2019
SwishPlus Implant 5.7mmD x 8mmL, SBM 6.5mmD Platform, Part Number 925708
FDA Recall
Terminated
·Implant Direct Sybron Manufacturing LLC·Product code NHA·January 9, 2019
Implant Direct, REF654311U, simply InterActive Implant, Surface: SBM, Qty 1, 4.3mmD x 11.5mmL, 3.4mmD Platform, RX only, Sterile R Dental Implant
FDA Recall
Terminated
·Implant Direct Sybron Manufacturing, LLC·Product code DZE·October 26, 2018
SwishPlus Implant Intended for use in support for fixed bridgework.
FDA Recall
Terminated
·Implant Direct Sybron Manufacturing, LLC·Product code NHA·January 19, 2018
SwishTapered Implant Intended for use in support for fixed bridgework.
FDA Recall
Terminated
·Implant Direct Sybron Manufacturing, LLC·Product code DZE·January 19, 2018