7 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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HOOK ELECTRODE, NEEDLE ELECTRODE, COAGULATION BUTTON ELECTRODE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
ALIF
FDA UDI
Nuvasive, Inc.·00887517839800·ALIF Blade, 60mm Reverse Tip
GENEX PUTTY
FDA 510(k)
FDA Class 2
·Orthopedic
Vivid E80, Vivid E90, Vivid E95
FDA 510(k)
FDA Class 2
·Radiology
OPTETRAK TIBIAL TRAY, FINNED, CEMENTED
FDA Adverse Event
Injury
·EXACTECH, INC·Product code JWH·August 5, 2015
NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM
FDA Adverse Event
Malfunction
·COCHLEAR LTD·Product code MCM·February 21, 2013
HARMONIC SCALPEL CURVED
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code GEI·August 1, 2014