7 results
·
22ms
·
Sources: EU EUDAMED, US FDA
TODAY PERSONAL LUBRICANT
FDA 510(k)
FDA Class 1
·General Hospital
NAR Kit
FDA UDI
NORTH AMERICAN RESCUE, LLC·00842209104994·KIT, NAR-4 AID w' COMBAT GAUZE - BLK - CUSTOM; ...
Livewire Electrophysiology Catheter
FDA 510(k)
FDA Class 2
·Cardiovascular
NOVABONE PUTTY - RESORBABLE BONE VOID FILLER
FDA 510(k)
FDA Class 2
·Orthopedic
GREENLIGHT XPS LASER SYSTEM
FDA Adverse Event
Malfunction
·AMERICAN MEDICAL SYSTEMS, INC. (SAN JOSE)·Product code GEX·June 5, 2014
ABSOLUTE PRO VASCULAR SELF-EXPANDING STENT SYSTEM
FDA Adverse Event
Malfunction
·AV-TEMECULA-CT·Product code NIO·November 29, 2012
OMNIPOD INSULIN PUMP
FDA Adverse Event
Injury
·INSULET CORPORATION·Product code LZG·September 29, 2010