7 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ISOLA OPEN AND CLOSED SCREWS
FDA 510(k)
FDA Class 2
·Orthopedic
ST FAMILY OF HOLLOW FIBER DIALYZERS
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
MATRICS
FDA 510(k)
FDA Class 1
·Ear, Nose, Throat
RESTORELLE DIRECTFIX POSTERIOR
FDA Adverse Event
Injury
·COLOPLAST A/S·Product code FTL·May 4, 2018
OBTRYX SYSTEM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·February 5, 2013
CARDIOVASCULAR PROCEDURE KIT
FDA Adverse Event
Malfunction
·TERUMO CARDIOVASCULAR SYSTEMS CORPORATION·Product code OEZ·December 10, 2010
UNKNOWN DEPUY PINNACLE SHELL
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL LTD. 8010379·Product code KWA·July 18, 2014