10,000 results · 33ms · Sources: EU EUDAMED, US FDA

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Neuspera SNM System

FDA UDI
NeuSpera Medical Inc.·00850075633418·Extra Lead

ELK LASER FILM DIGITIZER

FDA 510(k)
FDA Class 2 ·Radiology

Trina Turk

FDA UDI
MCGEE GROUP, INC., THE·00781096206087·Spectacle Frame, Size 52-17-135

Trina Turk

FDA UDI
MCGEE GROUP, INC., THE·00781096206094·Spectacle Frame, Size 52-17-135

ELK LASER IMAGER, MODEL EL-DRY 4000

FDA 510(k)
FDA Class 2 ·Radiology

EYEWEAR BY ROI BANNER ELK BLACK

FDA UDI
Eyewear By Roi, Limited·00748474521910·54-18-145 BLACK BULOVA EYEWEAR

EYEWEAR BY ROI BANNER ELK BLACK

FDA UDI
Eyewear By Roi, Limited·07484745219102·54-18-145 BLACK BULOVA EYEWEAR

DYNAGEN CRT-D

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code NIK·January 16, 2025

REPLACEMENT HEART VALVE

FDA Adverse Event
Injury ·EDWARDS LIFESCIENCES·Product code DYE·June 26, 2017

BD NEXIVA

FDA Adverse Event
Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·November 22, 2023

INFINION CX

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·June 23, 2020

UNKNOWN BATTERY POWERED HANDPIECES

FDA Adverse Event
Injury ·SYNTHES GMBH·Product code GEY·June 6, 2022

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·October 27, 2022

CONSTELLATION SURGICAL PROCEDURE PAK

FDA Adverse Event
Injury ·ALCON RESEARCH, LLC - HOUSTON·Product code LRO·June 8, 2021

UNKNOWN

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORPORATION·Product code GEX·October 29, 2024

HEARTWARE® VENTRICULAR ASSIST SYSTEM-PUMP

FDA Adverse Event
Death ·HEARTWARE, INC·Product code DSQ·August 15, 2017

HEARTWARE® VENTRICULAR ASSIST SYSTEM-PUMP

FDA Adverse Event
Injury ·HEARTWARE, INC·Product code DSQ·August 23, 2017

HEARTWARE® VENTRICULAR ASSIST SYSTEM - PUMP

FDA Adverse Event
Injury ·HEARTWARE·Product code DSQ·August 25, 2017

HEARTWARE® VENTRICULAR ASSIST SYSTEM - PUMP

FDA Adverse Event
Injury ·HEARTWARE·Product code DSQ·August 15, 2017

IMPLANTABLE NEUROSTIMULATOR

FDA Adverse Event
Injury ·MEDTRONIC NEUROMODULATION·Product code LGW·September 7, 2022