25 results · 24ms · Sources: EU EUDAMED, US FDA

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KLS Martin Individual Patient Solutions (IPS) Planning System

FDA 510(k)
FDA Class 2 ·Neurology

MEDI

FDA UDI
MEDI MANUFACTURING, INC.·04049772344093·PROTECT.PRO ACTION BACK SUPPORT BLACK S

Lockheed - 18 Metal

FDA UDI
Certified Safety Manufacturing, Inc.·00766588015026·Lockheed - 18 Metal

OsteoMed

FDA UDI
OSTEOMED LLC·00845694019385·HPS 1.6mm Screw & Plate Module

MED-TEC (MEDICAL INTELLIGENCE) BODYFIX SYSTEM, MODEL MT-BFX

FDA 510(k)
FDA Class 2 ·Radiology

MODEL GT010706 ELECTRONIC THERMOMETER

FDA 510(k)
FDA Class 2 ·General Hospital

BD VACUTAINER® SST¿ BLOOD COLLECTION TUBES

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO., (BD)·Product code JKA·January 4, 2023

Trilogy® Trabecular Metal®

FDA UDI
Zimmer, Inc.·00889024118508·

ANEURX STENT GRAFT SYSTEM

FDA Adverse Event
Death ·MEDTRONIC CARDIOVASCULAR·Product code MIH·February 18, 2011

TALENT ABDOMINAL STENT GRAFT SYSTEM

FDA Adverse Event
Injury ·MEDTRONIC CARDIOVASCULAR·Product code MIH·February 18, 2011

DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code QBJ·July 29, 2025

INRATIO

FDA Adverse Event
Malfunction ·ALERE SAN DIEGO, INC.·Product code GJS·July 1, 2011

PORTEX 8.0MM SUCTIONAID TRACHEOSTOMY TUBE

FDA Adverse Event
Malfunction ·SMITHS MEDICAL INTERNATIONAL LTD,·Product code BTO·September 16, 2014

QUICK COUPLING FOR K-WIRES

FDA Adverse Event
Malfunction ·SYNTHES GMBH·Product code HWE·July 2, 2013

ACCUSOL 35 5000ML (DRUG) (UK,IRELAND,POLAND,CZECH REP.,SLOV

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - CASTLEBAR·Product code KPO·October 19, 2010

ACCUSOL 35 5000ML (DRUG) (UK,IRELAND,POLAND,CZECH REP.,SLOV

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - CASTLEBAR·Product code KPO·October 19, 2010

ACCUSOL 35 5000ML (DRUG) (UK,IRELAND,POLAND,CZECH REP.,SLOV

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - CASTLEBAR·Product code KPO·October 27, 2010

ACCUSOL 35 5000ML (DRUG) (UK,IRELAND,POLAND,CZECH REP.,SLOV

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - CASTLEBAR·Product code KPO·October 27, 2010

NONE

FDA Adverse Event
Injury ·SYNTHES (USA)·Product code HWC·November 22, 2011

ONYX

FDA Adverse Event
Injury ·MICRO THERAPEUTICS, INC. DBA EV3·Product code MFE·October 2, 2024