18 results · 23ms · Sources: EU EUDAMED, US FDA

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Glass Ionomer Cement (Luting)

FDA 510(k)
FDA Class 2 ·Dental

VENTRALIGHT ST MESH

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

ZIRKONZAHN ICE

FDA 510(k)
FDA Class 2 ·Dental

AESCULAP SURGICAL INSTRUMENTS

FDA Adverse Event
Injury ·CHRISTOPH MIETHKE GMBH & CO. KG·Product code JXG·November 27, 2019

AESCULAP SURGICAL INSTRUMENTS

FDA Adverse Event
Injury ·CHRISTOPH MIETHKE GMBH & CO. KG·Product code JXG·November 27, 2019

Matrixx System

FDA UDI
NEXXT SPINE, LLC·00889929066126·Corpectomy, 16Dx18Wx51H 0°

Matrixx System

FDA UDI
NEXXT SPINE, LLC·00889929066430·Corpectomy, 16Dx18Wx51H 6°

MARATHON

FDA Adverse Event
Injury ·MEDTRONIC COVIDIEN·Product code KRA·March 30, 2017

ULTRAFLOW HPC

FDA Adverse Event
Injury ·MEDTRONIC COVIDIEN·Product code KRA·March 30, 2017

OLYMPUS EVIS EXERA II DUODENOVIDEOSCOPE

FDA Adverse Event
Injury ·OLYMPUS MEDICAL SYSTEMS CORPORATION·Product code FDT·June 7, 2013

ACCU-CHEK COMPACT TEST DRUM

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·July 14, 2011

CAPSUREFIX NOVUS

FDA Adverse Event
Injury ·MPRI·Product code DTB·October 10, 2014

PROGAV SYS PED.W/SA 15 A.PRECHAMBER

FDA Adverse Event
Injury ·CHRISTOPH MIETHKE GMBH & CO. KG·Product code JXG·April 4, 2019

CROSSCATH SUPPORT CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code KRA·March 6, 2019

CROSSCATH SUPPORT CATHETER

FDA Adverse Event
Injury ·COOK INC·Product code KRA·February 26, 2019

ONYX

FDA Adverse Event
Injury ·MICRO THERAPEUTICS, INC. DBA EV3 NEUROVA·Product code MFE·March 30, 2017

PROGAV 2.0 SYS PED.W/SA15 A.PRECHAMBER

FDA Adverse Event
Injury ·CHRISTOPH MIETHKE GMBH & CO. KG·Product code JXG·August 6, 2020

CROSSCATH SUPPORT CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code KRA·June 20, 2019