6 results
·
28ms
·
Sources: EU EUDAMED, US FDA
PODOSPRAY DRILL SYSTEM
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
MODEL 3873 1* 8 AND MODEL 3874 1* 8 COMPACT TEST STIMULATION LEADS
FDA 510(k)
FDA Class 2
·Neurology
CONCORDE Bullet Lumbar Interbody System
FDA 510(k)
FDA Class 2
·Orthopedic
CAPSUREFIX NOVUS
FDA Adverse Event
Malfunction
·MPRI·Product code DTB·February 9, 2013
SYNCHRON LX 20 CLINICAL SYSTEMS
FDA Adverse Event
Malfunction
·BECKMAN COULTER INC.·Product code JGS·January 6, 2011
TANDEM T:SLIM INSULIN DELIVERY SYSTEM
FDA Adverse Event
Injury
·TANDEM DIABETES CARE INC.·Product code LZG·July 2, 2014