10 results
·
30ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
BIPOLAR COAGULATING FORCEPS
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
DENTORIUM CONVERTIBLE ACRYLIC
FDA 510(k)
FDA Class 2
·Dental
SYNSTER CERVICAL CAGE, ALIF CAGE, PLIF CAGE, PTLIF CAGE, TLIF CAGE
FDA 510(k)
FDA Class 2
·Orthopedic
FREESTYLE FLASH
FDA Adverse Event
Malfunction
·ABBOTT DIABETES CARE, INC., USA·Product code LFR·October 24, 2007
INSYNC III MARQUIS
FDA Adverse Event
Injury
·MEDTRONIC S.A.·Product code NIK·October 31, 2012
SYSTEM CONSOLE
FDA Adverse Event
Malfunction
·DEPUY SYNTHES POWER TOOLS·Product code HBC·October 11, 2013
SCREW FIXATION BONE
FDA Adverse Event
Injury
·SYNTHES USA·Product code HWC·February 2, 2015
IMPLANT FIXATION DEVICE
FDA Adverse Event
Injury
·SYNTHES USA·Product code JDP·February 3, 2015
SCREW FIXATION BONE
FDA Adverse Event
Injury
·SYNTHES USA·Product code HWC·February 2, 2015
IMPLANT FIXATION DEVICE
FDA Adverse Event
Injury
·SYNTHES USA·Product code JDP·February 2, 2015