4,475 results · 30ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

ARRRAY SPINAL SYSTEM

FDA Adverse Event
Injury ·EBI·Product code KWQ·April 19, 2005

*

FDA Adverse Event
EBI·Product code HTY·September 24, 1997

EBI BONE HEALING SYSTEM

FDA Adverse Event
Injury ·EBI·Product code LOF·March 12, 2007

ARRAY SPINAL SYSTEM

FDA Adverse Event
Malfunction ·EBI·Product code NKB·February 21, 2007

ARRAY SPINAL SYSTEM

FDA Adverse Event
Malfunction ·EBI·Product code NKB·March 12, 2007

VUELOCK

FDA Adverse Event
Malfunction ·EBI·Product code KWQ·March 12, 2007

ARRAY SPINAL SYSTEM

FDA Adverse Event
Malfunction ·EBI·Product code NKB·March 6, 2007

SYNERGY

FDA Adverse Event
Malfunction ·EBI·Product code KWP·March 28, 2007

ARRAY SPINAL SYSTEM

FDA Adverse Event
Malfunction ·EBI·Product code NKB·February 20, 2007

ARRAY PEDICLE SCREW

FDA Adverse Event
Injury ·EBI·Product code MCV·March 27, 2006

ARRAY SPINE SYSTEM

FDA Adverse Event
Malfunction ·EBI,·Product code KWQ·March 15, 2006

BIOPLEX IMPLANT

FDA Adverse Event
Malfunction ·EBI·Product code JDK·October 17, 2007

PRO OSTEON 200R

FDA Adverse Event
Injury ·EBI·Product code MQV·November 9, 2007

PRO OSTEON 500

FDA Adverse Event
Malfunction ·EBI·Product code MQV·November 27, 2007

EBI VUELOCK ANTERIOR CERVICAL PLATE SYSTEM

FDA Adverse Event
Injury ·EBI·Product code KWQ·November 27, 2007

VHS SCREWDRIVER

FDA Adverse Event
Malfunction ·EBI·Product code HXX·October 17, 2007

VUELOCK SCREW INSERTER

FDA Adverse Event
Malfunction ·EBI·Product code HXX·October 1, 2007

POLARIS TORQUE INDICATING WRENCH

FDA Adverse Event
Malfunction ·EBI·Product code HXC·October 17, 2007

EBI ANTERIOR CERVICAL PLATE SYSTEM

FDA Adverse Event
Malfunction ·EBI.·Product code KWQ·December 6, 2007

ARRAY SPINAL SYSTEM

FDA Adverse Event
Injury ·EBI·Product code NKB·October 1, 2007