8 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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PS OMNIFIT NORMALIZED HIP STEM SERIES
FDA 510(k)
FDA Class 2
·Orthopedic
DeRoyal
FDA UDI
DEROYAL INDUSTRIES, INC.·00749756372107·EYE PACK
ADAPTIVE WEDGE
FDA 510(k)
FDA Class 2
·Orthopedic
MODIFICATION TO TISSUELINK MONOPOLAR FLOATING BALL
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
GMK SPHERE TOTAL KNEE SYSTEM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JWH·October 29, 2024
CONVEEN SECURITY URINE BAG, 500 ML, 50 CM TUBE
FDA Adverse Event
Injury
·COLOPLAST A/S·Product code FAQ·November 30, 2010
TELIGEN
FDA Adverse Event
Malfunction
·GUIDANT CRM CLONMEL IRELAND·Product code LWS·January 11, 2013
HOMECHOICE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - LARGO·Product code FKX·July 2, 2014