8 results
·
27ms
·
Sources: EU EUDAMED, US FDA
ACROMED SCREW DRIVER
FDA 510(k)
FDA Class 1
·Orthopedic
GC Initial™
FDA UDI
Gc America Inc.·J0228730661·GC Initial™ AL Dentin DD4, 20g
OSSEODUO Shaver and Drill System
FDA 510(k)
FDA Class 2
·Neurology
308 DERMATOLOGICAL EXCIMER SYSTEM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
UNKNOWN
FDA Adverse Event
Injury
·COOK INC·Product code KNT·April 17, 2020
CURVED SINUS BURS
FDA Adverse Event
Malfunction
·MDT PUERTO RICO OPERATIONS CO·Product code EQJ·June 13, 2014
PUMP MMT-722NAL PRDGM INS V2.2 CL EN PR
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO OPERATIONS MED-REL·Product code MDS·October 15, 2010
POWERED WHEELCHAIR
FDA Adverse Event
Malfunction
·INVACARE TAYLOR STREET·Product code ITI·December 13, 2012