8 results
·
19ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
SNAP BONE REAMER
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
KMEDIC
FDA UDI
TELEFLEX INCORPORATED·24026704262858·
Arthrex®
FDA UDI
ARTHREX, INC.·00888867060111·ARTHREX ECLIPSE HUMERAL HEAD, 53/22
A-DEC 2147 DOCTOR'S UNIT
FDA 510(k)
FDA Class 1
·Dental
MIDIGOLD 50
FDA 510(k)
FDA Class 2
·Dental
9800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·January 14, 2013
PROCEED MULTI-LAYER LAMINATE MESH
FDA Adverse Event
Injury
·ETHICON, INC.·Product code FTL·December 16, 2010
OT VERIO IQ METER
FDA Adverse Event
Injury
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 15, 2014