137 results · 81ms · Sources: EU EUDAMED, US FDA

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MERSILENE TAPE UNKNOWN PRODUCT

FDA Adverse Event
Injury ·ETHICON INC.·Product code KDC·November 20, 2018

NAIL,FIXATION,BONE

FDA Adverse Event
Injury ·SYNTHES USA·Product code JDS·July 19, 2016

SCREW,FIXATION,BONE

FDA Adverse Event
Malfunction ·SYNTHES USA·Product code HWC·July 19, 2016

APPLIANCE,FIXATION,NAIL

FDA Adverse Event
Injury ·SYNTHES USA·Product code KTT·April 26, 2017

SILK SUTURE UNKNOWN PRODUCT

FDA Adverse Event
Injury ·ETHICON INC.·Product code GAP·July 18, 2018

APPLIANCE,FIXATION,NAIL

FDA Adverse Event
Injury ·SYNTHES USA·Product code KTT·April 26, 2016

TENSION FREE VAGINAL TAPE UNKNOWN PRODUCT

FDA Adverse Event
Injury ·ETHICON INC.·Product code OTN·November 6, 2018

APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT

FDA Adverse Event
Injury ·SYNTHES USA·Product code KTT·April 26, 2016

TENSION FREE VAGINAL TAPE UNKNOWN PRODUCT

FDA Adverse Event
Injury ·ETHICON INC.·Product code OTN·October 5, 2018

GORE EXCLUDER AAA ENDOPROSTHESIS

FDA Adverse Event
Death ·W. L. GORE & ASSOCIATES, INC.·Product code MIH·February 24, 2021

PROLIFT PELVIC FLOOR REPAIR UNKNOWN PRODUCT

FDA Adverse Event
Injury ·ETHICON INC.·Product code OTP·September 21, 2018

LEVEEN¿ COACCESS¿

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC - COSTA RICA (COYOL)·Product code GEI·August 31, 2017

GORE EXCLUDER AAA ENDOPROSTHESIS

FDA Adverse Event
Death ·W. L. GORE & ASSOCIATES, INC.·Product code MIH·February 24, 2021

PLATE, FIXATION BONE

FDA Adverse Event
Injury ·SYNTHES USA·Product code HRS·February 9, 2015

PLATE, FIXATION BONE

FDA Adverse Event
Injury ·SYNTHES USA·Product code HRS·February 9, 2015

SCREW, FIXATION ,BONE

FDA Adverse Event
Malfunction ·SYNTHES USA·Product code HWC·February 9, 2015

THERMOCOOL SMARTTOUCH SF

FDA Adverse Event
Injury ·BIOSENSE WEBSTER INC·Product code LPB·September 3, 2025

THERMOCOOL SMARTTOUCH SF

FDA Adverse Event
Injury ·BIOSENSE WEBSTER INC·Product code LPB·September 3, 2025

KINETRA

FDA Adverse Event
Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·October 7, 2011

UNKNOWN DEEP BRAIN STIMULATOR

FDA Adverse Event
Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·May 18, 2011