9 results
·
26ms
·
Sources: EU EUDAMED, US FDA
NEXLOCK FEMORAL STEM
FDA 510(k)
FDA Class 2
·Orthopedic
MEXFLEX TOTAL HIP SYSTEM
FDA Adverse Event
Other
·ALPHATEC SPINE, INC.·Product code JDI·August 29, 2006
BASE
FDA UDI
Nuvasive, Inc.·00887517802729·BASE Ti Bolt, 5.0x17.5mm Fixed
3M™ Victory Series™
FDA UDI
3M UNITEK CORPORATION·00652221117991·3M™ Victory Series™ Second Molar Bands, 955-171...
TELEMETRY WAND MODEL
FDA 510(k)
FDA Class 3
·Cardiovascular
LOPEZ VALVE TM II
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
ATTAIN OTW
FDA Adverse Event
Injury
·MPRI·Product code LWP·February 11, 2013
DURATA STS OPTIM ACTIVE FIXATION, DF-4 CONNECTOR
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·January 10, 2011
PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)
FDA Adverse Event
Malfunction
·INVACARE FLORIDA OPERATIONS·Product code CAW·July 24, 2014