26 results
·
29ms
·
Sources: EU EUDAMED, US FDA
Navagio
FDA UDI
Kalitec Direct LLC·B07330K0134090·Trial, TLIF, 27L OB STR 7Deg, 9mm
AT HOME DRUG TEST, MODEL 9074
FDA 510(k)
FDA Unclassified
·Unknown
MAGNIVISION
FDA UDI
FGX INTERNATIONAL INC.·00024021566437·
STEVE MADDEN
FDA UDI
FGX INTERNATIONAL INC.·00193033484777·
MAGNIVISION
FDA UDI
FGX INTERNATIONAL INC.·00024021566451·
MAGNIVISION
FDA UDI
FGX INTERNATIONAL INC.·00024021566130·
STEVE MADDEN
FDA UDI
FGX INTERNATIONAL INC.·00193033484753·
STEVE MADDEN
FDA UDI
FGX INTERNATIONAL INC.·00193033484760·
MAGNIVISION
FDA UDI
FGX INTERNATIONAL INC.·00024021566468·
Navagio
FDA UDI
Kalitec Direct LLC·B07330K0132090·Trial, TLIF, 27L OB CRV 7Deg, 9mm
Navagio
FDA UDI
Kalitec Direct LLC·B07330K0134080·Trial, TLIF, 27L OB STR 7Deg, 8mm
CBC-SF
FDA 510(k)
FDA Class 2
·Hematology
ELECSYS FSH CALSET II
FDA 510(k)
FDA Class 2
·Clinical Chemistry
THERMACHOICE CATHETER UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code MNB·December 5, 2018
OMNIGUIDE BEAMPATH FIBER AND ADAPTER
FDA Adverse Event
OMNIGUIDE, INC.·Product code GEX·October 19, 2010
IBALANCE TKA TIBIAL TRAY SIZE 2
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code JWH·February 29, 2016
KOTEX NATURAL BALANCE
FDA Adverse Event
Injury
·KIMBERLY-CLARK CORPORATION - CONWAY MILL·Product code HEB·March 20, 2013
ALLURA XPER FD20
FDA Adverse Event
Malfunction
·PHILIPS HEALTHCARE·Product code IZI·February 2, 2011
ATTAIN OTW
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO, INC.·Product code LWP·March 10, 2008
2520274-2014-00875
FDA Adverse Event
Malfunction
·SYNTHES USA·Product code HRS·February 27, 2014