10,000 results · 127ms · Sources: EU EUDAMED, US FDA

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RESOLUTE INTEGRITY RX

FDA Adverse Event
Injury ·MEDTRONIC IRELAND·Product code NIQ·April 10, 2017

CPI ENDOTAC LEAD/CPK TRANSVERSE LEAD

FDA Adverse Event
Injury ·CARDIAC PACEMAKERS, INC.·Product code LWS·August 30, 1995

SPIDER RX

FDA Adverse Event
Injury ·COVIDIEN·Product code NFA·June 27, 2016

*

FDA Adverse Event
Injury ·*·Product code JXG·September 4, 1996

MO.MA

FDA Adverse Event
Injury ·INVATEC SPA·Product code NTE·June 27, 2016

CRAGG-MCNAMARA

FDA Adverse Event
Injury ·MICRO THERAPEUTICS, INC. DBA EV3·Product code KRA·May 3, 2022

JRNY II BCS FEMORAL OXIN RT SZ 5

FDA Adverse Event
Injury ·SMITH & NEPHEW, INC.·Product code JWH·September 9, 2025

1-DAY ACUVUE MOIST

FDA Adverse Event
Injury ·JOHNSON & JOHNSON VISION CARE, INC. ¿ US·Product code LPL·July 2, 2018

IN.PACT ADMIRAL PACLITAXEL-ELUTING PTA BALLOON CATHETER

FDA Adverse Event
Injury ·MEDTRONIC IRELAND·Product code ONU·September 29, 2016

ONYX

FDA Adverse Event
Injury ·MICRO THERAPEUTICS, INC. DBA EV3·Product code MFE·October 15, 2019

ENDEAVOR RX

FDA Adverse Event
Injury ·MEDTRONIC IRELAND·Product code NIQ·April 18, 2018

RESOLUTE INTEGRITY RX

FDA Adverse Event
Injury ·MEDTRONIC IRELAND·Product code NIQ·April 18, 2018

RESOLUTE INTEGRITY RX

FDA Adverse Event
Injury ·MEDTRONIC IRELAND·Product code NIQ·March 15, 2017

EVOLUT R TRANSCATHETER AORTIC VALVE

FDA Adverse Event
Injury ·MEDTRONIC HEART VALVES DIVISION·Product code NPT·June 22, 2017

COREVALVE REVALVING SYSTEM

FDA Adverse Event
Injury ·MEDTRONIC HEART VALVES DIVISION·Product code NPT·June 22, 2017

SPECTRA OPTIA

FDA Adverse Event
Injury ·TERUMO BCT·Product code LKN·August 12, 2024

HEARTMATE 3 LVAS IMPLANT KIT

FDA Adverse Event
Injury ·THORATEC CORPORATION·Product code DSQ·March 5, 2025

MEDTRONIC NAVIGATION

FDA Adverse Event
Injury ·MEDTRONIC NAVIGATION, INC·Product code HAW·January 6, 2025

UNKN. RT-PLUS MODULAR FEMORAL COMP.

FDA Adverse Event
Injury ·SMITH & NEPHEW ORTHOPAEDICS AG·Product code JWH·February 9, 2022

IMPELLA 5.0

FDA Adverse Event
Injury ·ABIOMED, INC.·Product code OZD·November 12, 2024