27 results
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32ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ACRYDERM SILVER ANTTIMICROBIAL WOUND GEL MODEL# A-002101
FDA 510(k)
FDA Unclassified
·Unknown
Henry Schein
FDA UDI
HENRY SCHEIN, INC.·00304040007983·Zirlux 16+ A4 89x17x12
Howard Leight
FDA UDI
SPERIAN HEARING PROTECTION, LLC·07312550119945·EARMUFF,LEIGHTNING L1N,NECKBND
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033366011·
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033366059·
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033365991·
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033366035·
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033366004·
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033366028·
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033366042·
TAKE ONE BITE MODIFIED
FDA 510(k)
FDA Class 2
·Dental
EEI SLUSH PAN DRAPE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
CRYOVALVE
FDA Adverse Event
Injury
·CRYOLIFE, INC.·Product code MIE·May 12, 1998
OT ULTRALINK METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 20, 2013
TRANSTAR STRETCHER
FDA Adverse Event
Malfunction
·HILL-ROM INC.·Product code FPO·February 14, 2011
ARTICUL/EZE ZIR BALL 28 +5
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC. 1818910·Product code LZO·August 15, 2014
MONOFOCAL IOLS
FDA Adverse Event
Injury
·ABBOTT MEDICAL OPTICS·Product code HQL·June 19, 2012
BD VACUTAINER® PUSH BUTTON BLOOD COLLECTION SET WITH PRE-ATTACHED HOLDER
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO., (BD)·Product code FMI·January 24, 2019
UNKNOWN GEL IMPLANTS
FDA Adverse Event
Injury
·MENTOR TEXAS·Product code FWM·April 17, 2018
REDUCTION FORCEPS WITH SERRATED JAW-RATCHET 144MM
FDA Adverse Event
Malfunction
·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HTD·October 31, 2019