8 results
·
23ms
·
Sources: EU EUDAMED, US FDA
TOMTECP90
FDA 510(k)
FDA Class 1
·Radiology
AXS-1 LITE WHEELCHAIR
FDA 510(k)
FDA Class 1
·Physical Medicine
RC-SwiftPrep
FDA 510(k)
FDA Unclassified
·Unknown
TITANIUM NEXGEN LCCL FEMORAL SZ C-LT
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·August 21, 2018
PLUM A+ UK WITH 3PIN
FDA Adverse Event
Malfunction
·HOSPIRA, INC.·Product code FRN·December 13, 2010
ASR UNI FEMORAL IMPL SIZE 43
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL·Product code KWA·February 8, 2013
PRONOVA* POLY (HEXAFLUOROPROPYLENE - VDF) SUTURE
FDA Adverse Event
Malfunction
·ETHICON INC.·Product code GAW·July 22, 2014
NEXGEN LEGACY POSTERIOR STABILIZED ARTICULAR SURFACE
FDA Adverse Event
Injury
·ZIMMER, INC.·Product code JWH·June 16, 2016