4,052 results · 26ms · Sources: EU EUDAMED, US FDA

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NFLEX CURV 1SEGM L55 PCU/TAV-ELI

FDA Adverse Event
Injury ·SYNTHES ELMIRA·Product code NQP·January 12, 2014

TI STENOFIX INTERSPINOUS IMPLANT 12MM-STERILE

FDA Adverse Event
Malfunction ·SYNTHES GMBH·Product code MNI·March 16, 2023

TI STENOFIX INTERSPINOUS IMPLANT 8MM-STERILE

FDA Adverse Event
Injury ·SYNTHES GMBH·Product code MNI·October 31, 2022

1030489-2016-03607

FDA Adverse Event
Malfunction ·MEDTRONIC SOFAMOR DANEK·Product code NQP·December 30, 2016

DYNESYS LIS, STABILIZING CORD, 100

FDA Adverse Event
Injury ·ZIMMER GMBH·Product code NQP·October 11, 2016

DYNESYS DTL SPACER CUTTER

FDA Adverse Event
Malfunction ·ZIMMER SPINE·Product code NQP·September 18, 2015

DYNESYS FUSION UNIVERSAL SPACER 6-45

FDA Adverse Event
Injury ·ZIMMER GMBH·Product code NQP·September 1, 2015

DYNESYS L.I.S. FUSION CORD 100

FDA Adverse Event
Injury ·ZIMMER GMBH·Product code NQP·September 1, 2015

ROD

FDA Adverse Event
Injury ·SYNTHES (USA)·Product code NQP·January 13, 2012

DYNESYS HA PEDICLE+SET SCREW 6.0X45

FDA Adverse Event
Injury ·ZIMMER GMBH·Product code NQP·March 29, 2012

DYNESYS IMPLANT GENERIC

FDA Adverse Event
Injury ·ZIMMER GMBH·Product code NQP·March 13, 2012

DYNESYS

FDA Adverse Event
Injury ·ZIMMER, INC.·Product code NQP·March 28, 2012

DYNESYS UNKNOWN

FDA Adverse Event
Injury ·ZIMMER, INC.·Product code NQP·March 23, 2012

6.5MM REVERE PEDICLE SCREW 50MM

FDA Adverse Event
Injury ·GLOBUS MEDICAL, INC.·Product code NQP·March 15, 2012

CD HORIZON AGILE SPINAL SYSTEM

FDA Adverse Event
Injury ·MEDTRONIC ORTHOPEDIC INC.·Product code NQP·March 19, 2009

CD HORIZON AGILE SPINAL SYSTEM

FDA Adverse Event
Malfunction ·WARSAW ORTHOPEDIC INC.·Product code NQP·February 12, 2009

N-HANCE ROD

FDA Adverse Event
Malfunction ·SYNTHES (USA)·Product code NQP·January 9, 2009

DYNESYS

FDA Adverse Event
Injury ·ZIMMER GMBH·Product code NQP·March 18, 2009

CD HORIZON AGILE SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDIC INC.·Product code NQP·February 5, 2009

CD HORIZON AGILE SPINAL SYSTEM

FDA Adverse Event
Malfunction ·WARSAW ORTHOPEDIC INC.·Product code NQP·February 5, 2009