25 results
·
30ms
·
Sources: EU EUDAMED, US FDA
ALGINATE FIBER
FDA 510(k)
FDA Unclassified
·Unknown
Master Series
FDA UDI
AMERICAN ORTHODONTICS CORPORATION·00190746100499·DB BKT MASTER LL CUSP 018 T=0 A+5 R=0
Sponge
FDA UDI
KATENA PRODUCTS, INC.·10841668111946·INSTRUMENT WIPE & CORNEAL SHIELD BX/20
6PW - Safety Award
FDA UDI
Certified Safety Manufacturing, Inc.·00766588050409·6PW - Safety Award
NexGen® Complete Knee Solution
FDA UDI
Zimmer, Inc.·00889024202368·
NexGen® Complete Knee Solution
FDA UDI
Zimmer, Inc.·00889024202351·
NexGen® Complete Knee Solution
FDA UDI
Zimmer, Inc.·00889024202344·
FORTRESS SPIRIT POWER WHEELCHAIR
FDA 510(k)
FDA Class 2
·Physical Medicine
TRAM PATIENT MONITOR
FDA 510(k)
FDA Class 2
·Cardiovascular
RUSCH 100% SIL TIEMANN 2WAY 5CC
FDA Adverse Event
Malfunction
·Product code EZL·May 27, 2014
TENDRIL ST
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVN·January 9, 2013
RENAL - DISPOSABLE
FDA Adverse Event
Injury
·Product code KDJ·November 22, 2010
BIOMET INTERLOK FIXED CRUCIATE TIBIAL PLATE
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·April 19, 2018
VANGUARD DCM PS TIBIAL BEARING
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·April 19, 2018
BIOMET MODULAR TIBIAL LOCKING BAR
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·April 19, 2018
VANGUARD 360 TIBIAL TRAY
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·April 19, 2018
BIOMET ARCOM PATELLA
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·April 19, 2018
BIOMET SMOOTH KNEE STEM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·April 19, 2018
VANGUARD POSTERIOR STABILIZED TIBIAL BEARING
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·April 19, 2018
VANGUARD TIBIAL CRUCIATE WING
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code MBH·April 19, 2018