6 results
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29ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MODIFICATION TO VF GEL PLUS
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
COBRA 1/2 FLEX SURGICAL PROBE, MODEL 1593X; COBRA FLEX SURGICAL PROBE MODEL 1594X
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
MODIFICATION TO SCIMED 6F IMPULSE ANGIOGRAPHIC CATHATERS
FDA 510(k)
FDA Class 2
·Cardiovascular
STRETCHER CHAIR
FDA Adverse Event
Malfunction
·STRYKER MEDICAL-KALAMAZOO·Product code FPO·April 26, 2013
CARPENTIER-EDWARDS PERIMOUNT MAGNA MITRAL PERICARDIAL BIOPROSTHESIS
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code DYE·May 8, 2011
XP1 SINGLE SYSTEM DENTAL IMPLANT
FDA Adverse Event
Injury
·KEYSTONE DENTAL·Product code DZE·July 23, 2008