7 results
·
17ms
·
Sources: EU EUDAMED, US FDA
D.O.R.C. VFI/VFE SYSTEM
FDA 510(k)
FDA Class 1
·Ophthalmic
DILATING TIP TROCAR WITH STABILITY SLEEVE - 12MM DIAMETER
FDA Adverse Event
Injury
·Product code GCJ·June 20, 2006
TECNOL SPLASHGUARD
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
GAUZE BANDAGE ROLL
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
ARTICULEZE M HEAD 36MM +1.5
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDIC INC, 1818910·Product code JDI·February 11, 2013
RIATA ST OPTIM ACTIVE FIXATION
FDA Adverse Event
Malfunction
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·January 10, 2011
EVOLUTION BILIARY CONTROLLED-RELEASE STENT- UNCOVERED
FDA Adverse Event
Injury
·COOK IRELAND LTD·Product code FGE·July 17, 2014