8 results
·
25ms
·
Sources: EU EUDAMED, US FDA
FREEMAN ACETABULAR CUP
FDA 510(k)
FDA Class 3
·Orthopedic
Lip Bumper
FDA UDI
AMERICAN ORTHODONTICS CORPORATION·00190746073328·LIP BUMPER 045 78MM SIZE 00
Apollo System
FDA 510(k)
FDA Class 2
·Neurology
VERSA-LINK PORCELAIN BONDING SYSTEM
FDA 510(k)
FDA Class 2
·Dental
APOLLO GENERATOR
FDA Adverse Event
Malfunction
·PENUMBRA, INC.·Product code GWG·June 11, 2015
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 6, 2014
CONTAK RENEWAL
FDA Adverse Event
Injury
·GUIDANT CRM CLONMEL IRELAND·Product code NIK·October 4, 2010
840 VENTILATOR
FDA Adverse Event
Malfunction
·COVIDIEN, FORMERLY NELLCOR PURITAN·Product code CBK·November 14, 2012