71 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Incontinence Treatment Device, Model LT2061
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B16741714300·
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B1674171430060·
NC Variobase Coping,screw-retained abutment
FDA UDI
BIO CONCEPT Co., Ltd.·06947600381495·
Ophthalmic Ring
FDA UDI
KATENA PRODUCTS, INC.·00841668100752·FLIERINGA FIXATION RING 14MM
MLS-AC DERMA SCANNER
FDA 510(k)
FDA Class 2
·Physical Medicine
SYNERAD OMNI, MODELS AN6255 AND AN6265
FDA 510(k)
FDA Class 2
·Radiology
INCORPORATE
FDA UDI
SPINAL ELEMENTS·00840606151900·17 X 14 CERVICAL TRIALS 30MM 0° LORDOSIS
INCORPORATE
FDA UDI
SPINAL ELEMENTS·00840606152099·17 X 14 CERVICAL TRIALS 30MM 10° LORDOSIS
EVOLUTION® BILIARY CONTROLLED-RELEASE STENT - FULLY COVERED
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code FCG·January 3, 2017
EVOLUTION® BILIARY CONTROLLED-RELEASE STENT - FULLY COVERED
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code FGE·February 2, 2016
EVOLUTION® BILIARY CONTROLLED-RELEASE STENT - FULLY COVERED
FDA Adverse Event
Injury
·COOK IRELAND LTD·Product code FGE·September 27, 2016
FGE CATHETER, BILIARY, DIAGNOSTIC - BILIARY STENT - METAL
FDA Adverse Event
Injury
·COOK INC·Product code FGE·January 29, 2020
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 15, 2013
KNIFE
FDA Adverse Event
Malfunction
·ALCON PRECISION DEVICE - SINKING SPRING·Product code HNN·June 30, 2011
ACCU-CHEK MULTICLIX LANCET
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code FMK·September 17, 2008
VC10 PUMP, 115V
FDA Adverse Event
Malfunction
·GYRUS ACMI, INC.·Product code HHK·January 2, 2025
EVOLUTION BILIARY CONTROLLED-RELEASE STENT-FULLY COVERED
FDA Adverse Event
Injury
·COOK IRELAND LTD·Product code FGE·March 25, 2015
EVOLUTION BILIARY CONTROLLED-RELEASE STENT - FULLY COVERED
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code FGE·April 24, 2015
EVOLUTION BILIARY CONTROLLED-RELEASE STENT - FULLY COVERED
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code FAD·March 12, 2015