55 results · 31ms · Sources: EU EUDAMED, US FDA

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LIGAMAX 5MM ENDO CLIP APPLIER

FDA Adverse Event
Injury ·ETHICON ENDO-SURGERY, LLC.·Product code FZP·May 5, 2014

CAPSUREFIX NOVUS

FDA Adverse Event
Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·October 15, 2012

FREESTYLE FLASH

FDA Adverse Event
Malfunction ·ABBOTT DIABETES CARE INC, USA·Product code LFR·July 26, 2007

ALINITY M RESP-4-PLEX AMP KIT

FDA Adverse Event
Malfunction ·ABBOTT MOLECULAR, INC.·Product code QJR·February 24, 2025

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
Death ·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 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
Death ·BIOSENSE WEBSTER, INC. (IRWINDALE)·Product code LPB·May 12, 2016

SIMILAR DEVICE NS7TCBL174HS, PMA # P990025

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