7 results
·
20ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
FINN KNEE PROSTHESIS
FDA 510(k)
FDA Class 2
·Orthopedic
DeRoyal
FDA UDI
DEROYAL INDUSTRIES, INC.·00749756379618·GENERAL MAJOR PACK
Juliet® Ti LL Lumbar Interbody Device
FDA 510(k)
FDA Class 2
·Orthopedic
CHEMWELL, MODEL 2900
FDA 510(k)
FDA Class 2
·Clinical Chemistry
TELIGEN
FDA Adverse Event
Malfunction
·GUIDANT CRM CLONMEL IRELAND·Product code LWS·January 11, 2013
TOTALCARE BARIATRIC
FDA Adverse Event
Malfunction
·HILL-ROM INC.·Product code FNL·November 23, 2010
DAILY ACTIVITY ASSIST DEVICES
FDA Adverse Event
LERADO·Product code ILS·July 2, 2014