6 results
·
23ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
Lancet
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
UNBALLOON NON-OCCLUSIVE MODELING CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
AART GLUTEAL IMPLANT
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
SENSOR ENLITE
FDA Adverse Event
Malfunction
·MEDTRONIC MINIMED·Product code OZO·November 3, 2014
3002 SECURE II
FDA Adverse Event
Malfunction
·STRYKER MEDICAL·Product code FNL·July 21, 2011
STELLARIS 23GA POSTERIOR PACK
FDA Adverse Event
Malfunction
·BAUSCH & LOMB, INC.·Product code HQC·July 9, 2013