31 results · 52ms · Sources: EU EUDAMED, US FDA

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PHOTODYNAMIC BONE STABILIZATION SYSTEM

FDA Adverse Event
Injury ·ILLUMINOSS MEDICAL, INC·Product code QAD·December 14, 2023

UNKNOWN VARIAX 2 VOLAR MEDIAL RIM DR PLATE, LONG

FDA Adverse Event
Injury ·STRYKER GMBH·Product code HRS·September 23, 2025

UNKNOWN INTACT CONSOLE

FDA Adverse Event
Injury ·MEDTRONIC ADVANCED ENERGY, LLC·Product code KNW·February 8, 2018

UNKNOWN INTACT HANDLE

FDA Adverse Event
Injury ·MEDTRONIC ADVANCED ENERGY, LLC·Product code KNW·February 8, 2018

UNKNOWN INTACT WAND

FDA Adverse Event
Injury ·MEDTRONIC ADVANCED ENERGY, LLC·Product code KNW·February 8, 2018

CORAIL2 STD SIZE 11

FDA Adverse Event
Injury ·DEPUY FRANCE SAS - 3003895575·Product code KWA·May 2, 2019

ESSURE

FDA Adverse Event
Injury ·BAYER PHARMA AG·Product code HHS·November 7, 2019

MESH - COMPOSIX

FDA Adverse Event
Death ·DAVOL INC., SUB. C.R. BARD, INC.·Product code FTL·January 19, 2011

S-ROM*SLEEVE PRX ZTT, 18B-SML

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS INC US·Product code LPH·December 4, 2019

PINN SECTOR W/GRIPTION 50MM

FDA Adverse Event
Injury ·Product code LPH·December 4, 2019

HEARTWARE VENTRICULAR ASSIST SYSTEM - DRIVELINE

FDA Adverse Event
Injury ·HEARTWARE, INC.·Product code DSQ·December 18, 2017

12/14 ARTICUL 44MM M SPEC+1.5

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS INC US·Product code LPH·February 16, 2023

HEARTWARE VENTRICULAR ASSIST SYSTEM-DRIVELINE

FDA Adverse Event
Injury ·HEARTWARE, INC.·Product code DSQ·July 6, 2018

AIGIS-R MEDIUM

FDA Adverse Event
Injury ·TYRX, INC.·Product code FTL·April 26, 2018

UPPER MODULE, COM1

FDA Adverse Event
Injury ·Product code OOK·April 15, 2020

ADAPTER SLEEVES 12/14 +2

FDA Adverse Event
Injury ·DEPUY INTERNATIONAL LTD - 8010379·Product code KWA·May 2, 2019

ARTEFILL DERMAL FILLER

FDA Adverse Event
Injury ·SUNEVA MEDICAL, INC.·Product code LMH·February 26, 2020

ACTIV.A.C.¿ ION PROGRESS¿ REMOTE THERAPY MONITORING SYSTEM

FDA Adverse Event
Injury ·KINETIC CONCEPTS, INC.·Product code OMP·December 13, 2021

PINN LNR CON +4 NEUT 28IDX50OD

FDA Adverse Event
Malfunction ·DEPUY ORTHOPAEDICS INC US·Product code KWZ·November 7, 2016

TURBO-POWER LASER ATHERECTOMY CATHETER

FDA Adverse Event
Malfunction ·SPECTRANETICS CORPORATION·Product code MCW·March 8, 2024