541 results · 22ms · 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.

HARMONIC HD 1000I SHEARS 36CM SHAFT

FDA Adverse Event
Injury ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·October 16, 2018

POWERED 60 ECHELON +, 440MM SHAFT

FDA Adverse Event
Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·March 14, 2023

POWERED 60 ECHELON +, 440MM SHAFT

FDA Adverse Event
Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·March 14, 2023

VICRYL POLYGLACTIN 910 SUTURE

FDA Adverse Event
Malfunction ·ETHICON INC.·Product code GAM·November 25, 2019

SIGMA STAB GVF INS 3 15MM

FDA Adverse Event
Injury ·JJM (SUZHOU) LTD. 3006356043·Product code JWH·December 13, 2018

PINN CAN BONE SCREW 6.5MMX30MM

FDA Adverse Event
Injury ·JJM (SUZHOU) LTD. 3006356043·Product code LPH·April 25, 2019

ARTICUL/EZE BALL 32 +5 BR

FDA Adverse Event
Injury ·JJM (SUZHOU) LTD. 3006356043·Product code JDI·May 2, 2019

PINN CAN BONE SCREW 6.5MMX25MM

FDA Adverse Event
Injury ·JJM (SUZHOU) LTD. 3006356043·Product code LPH·April 25, 2019

APEX HOLE ELIM POSITIVE STOP

FDA Adverse Event
Injury ·JJM (SUZHOU) LTD. 3006356043·Product code LPH·April 25, 2019

PFC*SIGMA/RD/DOME PAT 3PEG,35

FDA Adverse Event
Injury ·JJM (SUZHOU) LTD. 3006356043·Product code JWH·August 24, 2018

SIGMA STAB GVF INS 3 12.5MM

FDA Adverse Event
Malfunction ·JJM (SUZHOU) LTD. 3006356043·Product code JWH·August 22, 2018

APEX HOLE ELIM POSITIVE STOP

FDA Adverse Event
Injury ·JJM (SUZHOU) LTD. 3006356043·Product code LPH·March 18, 2019

PINN CAN BONE SCREW 6.5MMX15MM

FDA Adverse Event
Injury ·JJM (SUZHOU) LTD. 3006356043·Product code LPH·December 11, 2019

MOD T20 DRIVER SHORT

FDA Adverse Event
Malfunction ·DEPUY SYNTHES SPINE·Product code HWR·September 2, 2016

MICROSENSOR

FDA Adverse Event
Malfunction ·Product code GWM·August 25, 2016

CONFIDENCE KIT, NO NEEDLES

FDA Adverse Event
Malfunction ·DEPUY SYNTHES SPINE·Product code NDN·January 24, 2018

HS FOCUS 9CM PLUS ADAPTIVE

FDA Adverse Event
Injury ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·November 19, 2018

HARMONIC HD 1000I SHEARS 36CM SHAFT

FDA Adverse Event
Injury ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·December 13, 2018

UNKNOWN KNEE TIBIAL TRAY

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS, INC. 18189·Product code JWH·April 10, 2019

MOD T20 DRIVER SHORT

FDA Adverse Event
Malfunction ·DEPUY SYNTHES SPINE·Product code HWR·April 18, 2017