234 results · 32ms · 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.

GENESIS II

FDA Adverse Event
Injury ·SMITH & NEPHEW, INC. ORTHOPAEDIC DIVISION·Product code JWH·May 9, 2011

INTERVERTEBRAL FUSION DEVICE W/INTEGRATED FIXATION,CERVICAL

FDA Adverse Event
Injury ·OBERDORF : SYNTHES PRODUKTIONS GMBH·Product code OVE·January 16, 2018

KNEE-DUMMY IMPLANT

FDA Adverse Event
Injury ·SMITH & NEPHEW, INC.·Product code JWH·January 17, 2019

KNEE-DUMMY IMPLANT

FDA Adverse Event
Injury ·SMITH & NEPHEW, INC.·Product code JWH·January 10, 2019

KNEE-DUMMY IMPLANT

FDA Adverse Event
Injury ·SMITH & NEPHEW, INC.·Product code JWH·January 17, 2019

KNEE-DUMMY IMPLANT

FDA Adverse Event
Injury ·SMITH & NEPHEW, INC.·Product code JWH·January 17, 2019

TRANSFORM

FDA Adverse Event
Injury ·MEDTRONIC, INC.·Product code LDK·April 10, 2018

KNEE-DUMMY IMPLANT

FDA Adverse Event
Injury ·SMITH & NEPHEW, INC.·Product code JWH·October 23, 2019

KNEE-DUMMY IMPLANT

FDA Adverse Event
Injury ·SMITH & NEPHEW, INC.·Product code JWH·October 23, 2019

KNEE-DUMMY IMPLANT

FDA Adverse Event
Injury ·SMITH & NEPHEW, INC.·Product code JWH·October 23, 2019

KNEE-DUMMY IMPLANT

FDA Adverse Event
Injury ·SMITH & NEPHEW, INC.·Product code JWH·October 23, 2019

UNKN GENESIS II TOTAL KNEE FEM COMP COCR CEM

FDA Adverse Event
Injury ·SMITH & NEPHEW, INC.·Product code HRY·June 13, 2022

UNKN GENESIS II TOTAL KNEE TIB INSERT

FDA Adverse Event
Injury ·SMITH & NEPHEW, INC.·Product code HRY·June 11, 2022

ORTHOSIS, PEDICLE SPINAL FIXATION, FOR DDD

FDA Adverse Event
Injury ·SYNTHES USA·Product code NKB·September 10, 2015

ORTHOSIS, PEDICLE SPINAL FIXATION, FOR DDD

FDA Adverse Event
Injury ·SYNTHES USA·Product code NKB·September 10, 2015

ORTHOSIS, PEDICLE SPINAL FIXATION, FOR DDD

FDA Adverse Event
Malfunction ·SYNTHES USA·Product code NKB·September 10, 2015

ORTHOSIS, PEDICLE SPINAL FIXATION, FOR DDD

FDA Adverse Event
Injury ·SYNTHES USA·Product code NKB·September 10, 2015

ORTHOSIS, PEDICLE SPINAL FIXATION, FOR DDD

FDA Adverse Event
Malfunction ·SYNTHES USA·Product code NKB·September 10, 2015

BD SYR MF 1CC 1S 28G

FDA Adverse Event
Malfunction ·BDK·Product code FMF·January 20, 2010

SKYTRON

FDA Adverse Event
Malfunction ·DDK·Product code FSY·October 21, 2014