24 results
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28ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SOPRO 67D OPERATING ROOM CAMERA
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
Henry Schein
FDA UDI
HENRY SCHEIN, INC.·00304040047828·Curette Gracey DE 17/18
ALPHATEC
FDA Adverse Event
ALPHATEC MFG INC. AKA NEXMED INC·Product code HWC·February 26, 2004
MATIRA ANTERIOR CERVICAL SYSTEM
FDA UDI
Kalitec Direct LLC·B07307K0130001·PLATE BENDER, UNIVERSAL
CorticaLINK
FDA UDI
LINKSPINE, INC.·00817329022497·Ti Rod - Curved - 90mm
BETHENNY EYEWEAR
FDA UDI
FGX INTERNATIONAL INC.·00193033456231·
BETHENNY EYEWEAR
FDA UDI
FGX INTERNATIONAL INC.·00193033456248·
BETHENNY EYEWEAR
FDA UDI
FGX INTERNATIONAL INC.·00193033456255·
BETHENNY EYEWEAR
FDA UDI
FGX INTERNATIONAL INC.·00193033456224·
Patient Circuit
FDA UDI
FLIGHT MEDICAL INNOVATIONS LTD·17290013641288·F60 DL Flow Sensor Kit
BETHENNY EYEWEAR
FDA UDI
FGX INTERNATIONAL INC.·00193033456200·
BETHENNY EYEWEAR
FDA UDI
FGX INTERNATIONAL INC.·00193033456194·
BETHENNY EYEWEAR
FDA UDI
FGX INTERNATIONAL INC.·00193033456217·
XLTEK EVOKED POTENTIAL HEADBOX, MODEL EP-4-RP (PROPOSED)
FDA 510(k)
FDA Class 2
·Neurology
MIDMARK PROCENTER INSTRUMENT DELIVERY SYSTEM
FDA 510(k)
FDA Class 1
·Dental
ACIST
FDA Adverse Event
Injury
·ACIST MEDICAL SYSTEMS, INC.·Product code DXT·February 10, 2012
TAXUS® LIBERTÉ®
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - MAPLE GROVE·Product code NIQ·March 20, 2013
RESTYLANE-L INJECTABLE GEL
FDA Adverse Event
Other
·Q-MED AB·Product code LMH·March 2, 2011
HEART CONTINUOUS NEBULIZER
FDA Adverse Event
Injury
·WESTMED·Product code CAF·March 11, 2008
ACIST
FDA Adverse Event
Malfunction
·ACIST MEDICAL SYSTEMS, INC.·Product code DXT·April 20, 2007