439 results · 46ms · Sources: EU EUDAMED, US FDA

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EVIS LUCERA ELITE BRONCHOVIDEOSCOPE

FDA Adverse Event
Injury ·AIZU OLYMPUS CO., LTD.·Product code EOQ·July 25, 2023

THORATEC® HEARTMATE 3® LVAS IMPLANT KIT

FDA Adverse Event
Injury ·THORATEC CORPORATION·Product code DSQ·January 9, 2025

PREMILENE/MONOSYN SET

FDA Adverse Event
Malfunction ·B.BRAUN SURGICAL S.A.·Product code GAW·August 7, 2015

INOMAX DS (DELIVERY SYSTEM)

FDA Adverse Event
Injury ·INO THERAPEUTICS LLC.IKARIA·Product code MRN·November 16, 2011

INOMAX DE (DELIVERY SYSTEM)

FDA Adverse Event
Malfunction ·INO THERAPEUTICS LLC / IKARIA·Product code MRN·July 30, 2010

PINN MAR NEUT 28IDX46OD

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS INC US·Product code LPH·August 21, 2020

SPYSCOPE DS II ACCESS & DELIVERY CATHETER

FDA Adverse Event
Death ·BOSTON SCIENTIFIC CORPORATION·Product code FBN·December 22, 2025

AMPLATZ SUPER STIFF

FDA Adverse Event
Death ·BOSTON SCIENTIFIC CORPORATION·Product code DQX·January 29, 2026

MICRA

FDA Adverse Event
Malfunction ·MEDTRONIC IRELAND·Product code PNJ·January 11, 2021

LUPINE BR DS W/ORTHCRD

FDA Adverse Event
Malfunction ·DEPUY MITEK LLC US·Product code MAI·April 1, 2024

FUKUDA DENSHI MODEL DS-5700 CENTRAL STATION

FDA Adverse Event
Malfunction ·FUKUDA DENSHI CO., LTD.·Product code DSI·December 15, 2004

NAVITOR VISION

FDA Adverse Event
Injury ·ABBOTT MEDICAL·Product code NPT·June 27, 2025

CANDELA GENTLEMAX LASER SYSTEM

FDA Adverse Event
Malfunction ·CANDELA CORPORATION·Product code GEX·April 7, 2017

NAVITOR TRANSCATHETER AORTIC VALVE

FDA Adverse Event
Injury ·ABBOTT MEDICAL·Product code NPT·April 16, 2026

FLEXNAV DELIVERY SYSTEM

FDA Adverse Event
Injury ·ABBOTT MEDICAL·Product code NPT·October 31, 2025

FLEXNAV DELIVERY SYSTEM

FDA Adverse Event
Malfunction ·ABBOTT MEDICAL·Product code NPT·September 16, 2025

INOMAX DS (DELIVERY SYSTEM)

FDA Adverse Event
Injury ·INO THERAPEUTICS LLC/ IKARIA·Product code MRN·December 20, 2011

IOLMASTER 500

FDA Adverse Event
Injury ·CARL ZEISS MEDITEC AG·Product code HJO·July 17, 2014

STOCKERT 70 RF GENERATOR

FDA Adverse Event
Injury ·STOCKERT GMBH·Product code DRF·December 28, 2011

SPECTRUM IQ

FDA Adverse Event
Malfunction ·BAXTER INTERNATIONAL INC.·Product code FRN·August 30, 2024