15 results · 19ms · 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.

TAXUS EXPRESS2 PACLITAXEL-ELUTING CORONARY STENT SYSTEM

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC·Product code NIQ·June 21, 2007

LOW PROF SCRW,SS 4.0X 45MMCANN,SHT THD

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code HWC·September 27, 2023

DRV SFT,CANN,QC,T15 HEXALOBE

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code MDM·September 27, 2023

LO-PRO SCRW,TI,3.0MMX 20MMCORT

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code HWC·August 16, 2023

LO-PRO SCRW,TI,3.5MMX 12MM

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code HRS·August 17, 2023

3.0 X 14MM VAL SCREW, TI

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code HWC·August 17, 2023

3.0 X 16MM VAL SCREW, TI

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code HWC·August 17, 2023

3.0 X 18MM VAL SCREW, TI

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code HWC·August 17, 2023

LOCKING DISTAL FIBULA PLATE, TI ,LEFT,4H

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code HRS·August 17, 2023

3.0 X 20MM VAL SCREW, TI

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code HWC·August 17, 2023

LO-PRO SCRW,TI,3.5MMX 26MM

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code HWC·August 17, 2023

K-LESS T-ROPE W/DRV, SYN REPR, TI

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code HTN·August 16, 2023

LO-PRO SCRW,TI,3.5MMX 14MM

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code HWC·August 17, 2023

3.0 X 12MM VAL SCREW, TI

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code HWC·August 16, 2023

LO-PRO SCRW,TI,3.5MMX 14MM

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code HWC·August 17, 2023