9 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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HEADLOC CERAMIC FEMORAL HEADS
FDA 510(k)
FDA Class 2
·Orthopedic
PEEK Corpectomy
FDA UDI
Nuvasive, Inc.·00887517623904·PEEK Corp Core, Ø14x35mm
VirtuOst Vertebral Fracture Assessment
FDA 510(k)
FDA Class 2
·Radiology
NUVASIVE OCT SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
GREENLIGHT MOXY FIBER OPTIC
FDA Adverse Event
Malfunction
·AMS·Product code GEX·February 4, 2013
UNKNOWN DEPUY FEMORAL HEAD
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL LTD. 8010379·Product code KWA·July 31, 2014
MALLINCKRODT
FDA Adverse Event
Injury
·COVIDIEN, FORMERLY TYCOHEALTHCARE·Product code BTR·January 20, 2011
SINGLE FUNCTION ABC PENCIL, HAND CONTROL HANDPIECE
FDA Adverse Event
Malfunction
·CONMED ELECTROSURGERY·Product code HAM·September 11, 2015
ABC HANDPIECE LAPAROSCOPIC
FDA Adverse Event
Malfunction
·CONSOLIDATED MEDICAL EQUIPMENT·Product code HAM·February 19, 2019