54 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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POLARIS PRESSURE ADJUSTABLE VALVE SYSTEM/POLARIS ADJUSTABLE VALVE WITH SIPHONX
FDA 510(k)
FDA Class 2
·Neurology
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04049772814305·GENUMEDI PT SILVER R VII
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04049772814244·GENUMEDI PT SILVER L VII
BIOMET KNEE SYSTEM
FDA UDI
Biomet Orthopedics, LLC·00880304231900·
Biomet® Knee System
FDA UDI
Biomet Orthopedics, LLC·00887868558634·
Biomet® Knee System
FDA UDI
Biomet Orthopedics, LLC·00887868247910·
MODIFICATION TO:ROCHE DIAGNOSTICS PRECINORM UNIVERSAL AND PRECIPATH UNIVERSAL CONTROL SERA
FDA 510(k)
FDA Class 1
·Clinical Chemistry
BACK-TEK
FDA 510(k)
FDA Class 2
·Physical Medicine
ONE TOUCH ULTRA
FDA Adverse Event
Malfunction
·LIFESCAN, INC.·Product code NBW·January 3, 2006
PARADIGM REAL-TIME INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·October 3, 2014
CHISEL F/FOOT STRAIG NARR W/10 L124
FDA Adverse Event
Malfunction
·SYNTHES GMBH·Product code FZO·June 3, 2013
TRI-LOCK BPS SZ 4 STD OFFSET
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code KWA·June 22, 2011
VGD CRUC RET TIB BRG 11X87/91
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·August 7, 2018
VANGUARD CR ILOK FEMORAL
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·August 7, 2018
ARCOM SERIES A STANDARD PATELLA
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·August 9, 2018
VNGD CR LIP TIB BRG 14X87/91MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·August 9, 2018
VANGUARD CR ILOK FEM-RT 75
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·August 9, 2018
BIOMET CC I-BEAM TRAY 87MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·August 9, 2018
VNGD CR TIB BRG 10X87/91
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·August 8, 2018
HF UNIT "ESG-400"
FDA Adverse Event
Malfunction
·OLYMPUS WINTER & IBE GMBH·Product code GEI·April 23, 2021