10 results
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38ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
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COCHLEAR¿ NUCLEUS® NEXA® COCHLEAR IMPLANT WITH SLIM MODIOLAR ELECTRODE
FDA Adverse Event
Injury
·COCHLEAR LIMITED·Product code MCM·February 13, 2026
COCHLEAR¿ NUCLEUS® NEXA® COCHLEAR IMPLANT WITH CONTOUR ADVANCE® ELECTRODE
FDA Adverse Event
Injury
·COCHLEAR LTD·Product code MCM·February 13, 2026
NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM
FDA Adverse Event
Injury
·COCHLEAR LTD.·Product code MCM·May 24, 2013
COCHLEAR OSIA OSI300 IMPLANT
FDA Adverse Event
Injury
·COCHLEAR LIMITED·Product code PFO·January 15, 2024
NUCLEUS 24 CHANNEL HYBRID COCHLEAR IMPLANT SYSTEM
FDA Adverse Event
Injury
·COCHLEAR LTD·Product code PGQ·July 4, 2016
NUCLEUS 24 CHANNEL HYBRID COCHLEAR IMPLANT SYSTEM
FDA Adverse Event
Malfunction
·COCHLEAR LTD.·Product code PGQ·August 1, 2016
LUMBER INTERBODY FUSION SYSTEM INSTRUMENTATION
FDA Adverse Event
Injury
·CENTERPULSE SPINE-TECH·Product code LXH·December 11, 2003
DAILY ACTIVITY ASSIST DEVICES
FDA Adverse Event
UNKNOWN·Product code IKX·February 20, 2013
OT ULTRALINK METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 31, 2014
PROGRAMMING SOFTWARE
FDA Adverse Event
Malfunction
·CYBERONICS, INC.·Product code LYJ·January 14, 2011