42 results · 21ms · Sources: EU EUDAMED, US FDA

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NUCLEUS 22

FDA Adverse Event
Injury ·COCHLEAR LIMITED·Product code MCM·May 18, 2025

ARROW

FDA Adverse Event
Injury ·CODMAN & SHURTLEFF·Product code LKK·July 25, 2023

CODMAN 3000

FDA Adverse Event
Injury ·CODMAN & SHURTLEFF·Product code LKK·July 28, 2023

CODMAN 3000

FDA Adverse Event
Injury ·CODMAN & SHURTLEFF·Product code LKK·July 20, 2023

BIOCOMP. INTERFERENCE SCREW, FULL THREAD

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code MAI·June 24, 2014

ENDO GIA UNIVERSAL 12MM SINGLE USE INST

FDA Adverse Event
Injury ·UNITED STATES SURGICAL·Product code GDW·November 1, 2010

SIMILAR DEVICE NS7TCBL174HS, PMA # P990025

FDA Adverse Event
Injury ·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code LPB·July 17, 2015

SIMILAR DEVICE NS7TCBL174HS, PMA # P990025

FDA Adverse Event
Injury ·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code LPB·July 20, 2015

SIMILAR DEVICE NS7TCBL174HS, PMA # P990025

FDA Adverse Event
Injury ·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code LPB·July 20, 2015

SIMILAR DEVICE NS7TCBL174HS, PMA # P990025

FDA Adverse Event
Injury ·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code LPB·July 20, 2015

SIMILAR DEVICE NS7TBL174HS, PMA # P990025

FDA Adverse Event
Injury ·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code LPB·November 10, 2014

SIMILAR DEVICE NS7TCBL174HS, PMA # P990025

FDA Adverse Event
Injury ·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code LPB·July 20, 2015

SIMILAR DEVICE NS7TCBL174HS, PMA # P990025

FDA Adverse Event
Injury ·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code LPB·July 20, 2015

SIMILAR DEVICE NS7TCBL174HS, PMA # P990025

FDA Adverse Event
Injury ·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code DRF·March 5, 2015

SIMILAR DEVICE NS7TCBL174HS, PMA # P990025

FDA Adverse Event
Injury ·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code DRF·March 4, 2015

SIMILAR DEVICE NS7TCBL174HS, PMA # P990025

FDA Adverse Event
Injury ·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code DRF·February 6, 2015

SIMILAR DEVICE NS7TCBL174HS, PMA # P990025

FDA Adverse Event
Injury ·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code DRF·March 4, 2015

SIMILAR DEVICE NS7TCBL174HS, PMA # P990025

FDA Adverse Event
Injury ·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code LPB·March 6, 2015

SIMILAR DEVICE NS7TCBL174HS, PMA # P990025

FDA Adverse Event
Injury ·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code DRF·February 13, 2015

SIMILAR DEVICE NS7TCBL174HS, PMA # P990025

FDA Adverse Event
Injury ·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code LPB·April 23, 2015