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LapWrap® / TrenMAX

FDA UDI
Innovative Medical Products, Inc·00696588003566·LapWrap®/TrenMAX™ Extensions (10 - 4 packs per ...

SCHNEIDER MONORAIL-GEX(TM) GUIDEWIRE EXCHANGE CATH

FDA 510(k)
FDA Class 2 ·Cardiovascular

Humbles LapWrap®

FDA UDI
Innovative Medical Products, Inc·00696588005997·Humbles LapWrap® Extensions Sample

SCHNEIDER GEX(TM) .014/.018 GUIDEWIRE EXCHANGE CATHETER

FDA 510(k)
FDA Class 2 ·Cardiovascular

GE OEC 9800

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·October 23, 2009

INNOVA 21 EPI

FDA Adverse Event
Malfunction ·GE MEDICAL SYSTEMS, LLC·Product code JAA·April 4, 2023

GE OEC 9600

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·December 15, 2008

OPTICAL FIBER 200 MICRON STANDARD SINGLE USE

FDA Adverse Event
Injury ·QUANTA SYSTEM S.P.A·Product code GEX·April 15, 2022

GEX LASER INSTRUMENT, SURGICAL

FDA Adverse Event
Malfunction ·COOK INC·Product code GEX·March 4, 2019

GEX LASER INSTRUMENT, SURGICAL

FDA Adverse Event
Malfunction ·COOK INC·Product code GEX·August 1, 2018

UNKNOWN

FDA Adverse Event
Death ·KARL STORZ SE & CO. KG·Product code GEX·March 20, 2025

ALOCC

FDA Adverse Event
Malfunction ·GE MEDICAL SYSTEMS·Product code KPR·November 27, 2007

ALLIA

FDA Adverse Event
Malfunction ·GE HEALTHCARE TECHNOLOGIES, INC.·Product code OWB·January 22, 2026

XT RADIOGRAPHIC SUSPENSION

FDA Adverse Event
Malfunction ·GENERAL ELECTRIC MEDICAL SYSTEMS·Product code IYB·August 19, 1999

AVE GFX OTW CORONARY STENT SYSTEM

FDA Adverse Event
Injury ·ARTERIAL VASCULAR ENGINEERING, INC.·Product code MAF·May 15, 1998

PRECISION SPECTRA

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·December 26, 2017

QUANTA SYSTEM

FDA Adverse Event
Malfunction ·QUANTA SYSTEM, S.P.A·Product code GEX·February 18, 2026

IMAG PAD UNIVERSAL GE X-RAY NAR, CC/SEAMLESS VIN TEAL

FDA UDI
ALIMED, INC.·00733657259209·

GORE-TEX SUTURE CV5

FDA Adverse Event
Injury ·W.L. GORE & ASSOCIATES·Product code DTH·April 30, 2009

VL 45CM KIT (FIBER), PRODUCT CODE GEX

FDA Adverse Event
Malfunction ·VASCULAR SOLUTIONS, INC.·Product code GEX·December 17, 2008