6 results
·
26ms
·
Sources: EU EUDAMED, US FDA
OTOLOGICAL VENTILATION TUBES
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
Electrical Stimulator - Model R-C1 TENS and EMS stimulator, Model R-E1 EMS stimulator, Model R-T1 TENS Stimulator
FDA 510(k)
FDA Class 2
·Neurology
MODIFICATION TO VF GEL PLUS
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
FULL OSSEOTITE® IMPLANT 4 X 13MM
FDA Adverse Event
Injury
·BIOMET 3I·Product code DZE·April 30, 2014
RESOLUTE INTEGRITY RX
FDA Adverse Event
Malfunction
·MEDTRONIC, INC.·Product code NIQ·September 18, 2012
MINIARC SLING SYSTEMS
FDA Adverse Event
Injury
·AMERICAN MEDICAL SYSTEMS, INC.·Product code FTL·July 27, 2010