6 results
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18ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ANCHOR BRAND SURGICAL NEEDLES
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
Muscle Stimulator
FDA 510(k)
FDA Class 2
·Neurology
VISERA RHINO-LARYNGOVIDEOSCOPE OLYMPUS ENF TYPE V
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
6.0MM TI MATRIX REDUCTION SCREW 40MM THREAD LENGTH
FDA Adverse Event
Injury
·SYNTHES BRANDYWINE·Product code NKB·May 26, 2014
GREENLIGHT MOXY FIBER OPTIC
FDA Adverse Event
Injury
·AMERICAN MEDICAL SYSTEMS·Product code GEX·November 9, 2012
CAPSUREFIX NOVUS
FDA Adverse Event
Death
·MEDTRONIC PUERTO RICO, INC.·Product code DTB·September 13, 2010