26 results
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28ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MOST OPTIONS SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
Xltek
FDA UDI
Embla Systems Ltd·00382830023771·Embletta MPR ST Proxy
MAGNIVISION
FDA UDI
FGX INTERNATIONAL INC.·00193033588499·
MAGNIVISION
FDA UDI
FGX INTERNATIONAL INC.·00193033588475·
Intess L
FDA UDI
Kalitec Direct LLC·B07312K0100310·Assembly,Caddie, Lumbar Implants, Hinged
MAGNIVISION
FDA UDI
FGX INTERNATIONAL INC.·00193033588482·
MAGNIVISION
FDA UDI
FGX INTERNATIONAL INC.·00193033588505·
Matira
FDA UDI
Kalitec Direct LLC·B073DRK010031·Drill Guide, Straight, Featureless, Amann
MAGNIVISION
FDA UDI
FGX INTERNATIONAL INC.·00193033588468·
Inseption
FDA UDI
Kalitec Direct LLC·B07314K0100310·Assembly, Caddie, ISP Implants, Hinged
MAGNIVISION
FDA UDI
FGX INTERNATIONAL INC.·00193033588512·
Cosmolock
FDA UDI
Kalitec Direct LLC·B07311K0130110·Segmental Rod Reducer, Slim, Assembly
Kalitec Disc Prep
FDA UDI
Kalitec Direct LLC·B07319K0160310·Curette, Forward Angle, #5
DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·August 25, 2021
LENSOCLEAN MULTI-PURPOSE SOLUTION, MODEL 355ML
FDA 510(k)
FDA Class 2
·Ophthalmic
NANODUCT NEONATAL SWEAT ANALYSIS SYSTEM
FDA 510(k)
FDA Class 2
·Physical Medicine
VITEK® 2 GP TEST KIT
FDA Adverse Event
Malfunction
·BIOMERIEUX, INC.·Product code LQL·August 28, 2018
SCHILLER
FDA Adverse Event
Malfunction
·SCHILLER AG·Product code MHX·November 2, 2006
2800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·March 1, 2013
UNKNOWN DEPUY ASR 50 CUP
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL, LTD.·Product code KWA·February 24, 2011