18 results
·
23ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
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