1,319 results
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70ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
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ABC SELF-LOCKING CERVICAL SCREW 4.0X16MM
FDA Adverse Event
Malfunction
·AESCULAP AG & CO. KG·Product code KWQ·July 17, 2010
PROSTHESIS, INTERVERTEBRAL DISC
FDA Adverse Event
Injury
·SYNTHES USA·Product code MJO·October 26, 2016
PROSTHESIS, INTERVERTEBRAL DISC
FDA Adverse Event
Injury
·SYNTHES USA·Product code MJO·October 26, 2016
PROSTHESIS, INTERVERTEBRAL DISC
FDA Adverse Event
Malfunction
·SYNTHES USA·Product code MJO·October 26, 2016
PROSTHESIS, INTERVERTEBRAL DISC
FDA Adverse Event
Injury
·SYNTHES USA·Product code MJO·October 26, 2016
PROSTHESIS, INTERVERTEBRAL DISC
FDA Adverse Event
Injury
·SYNTHES USA·Product code MJO·October 26, 2016
PROSTHESIS, INTERVERTEBRAL DISC
FDA Adverse Event
Malfunction
·SYNTHES USA·Product code MJO·October 26, 2016
PROSTHESIS, INTERVERTEBRAL DISC
FDA Adverse Event
Malfunction
·SYNTHES USA·Product code MJO·October 26, 2016
CASPAR DISTR PIN16MMSTER
FDA Adverse Event
Malfunction
·AESCULAP AG & CO. KG·Product code LXH·August 21, 2008
BICONTACT S COCR CEMENTED 12/14 SZ.10MM
FDA Adverse Event
Malfunction
·AESCULAP AG & CO. KG·Product code LWJ·April 5, 2012
BICONTACT S PLASMAPORE 12/14 SIZE 17MM
FDA Adverse Event
Malfunction
·AESCULAP AG & CO. KG·Product code JWH·April 27, 2012
COLLECT.NO.QAS KNEE IMPLANTS COLUMBUS
FDA Adverse Event
Injury
·AESCULAP AG·Product code JWH·January 29, 2025
THREADED PIN HEADLESS 3.2MM X 63MM
FDA Adverse Event
Malfunction
·AESCULAP AG & CO. KG·Product code LXH·May 29, 2009
BICONTACT S COCR CEMENTED 12/14 SZ.16MM
FDA Adverse Event
Malfunction
·AESCULAP AG & CO. KG.·Product code LWJ·April 27, 2012
AS TIBIA EXTENSION STEM 10X52MM CEMENTED
FDA Adverse Event
Injury
·AESCULAP AG·Product code JWH·April 30, 2026
VEGA PS+ GLIDING SURFACE T2/2+ 14MM
FDA Adverse Event
Injury
·AESCULAP AG·Product code JWH·April 30, 2026
AS VEGA PS TIBIAL PLATEAU CEMENTED T2+
FDA Adverse Event
Injury
·AESCULAP AG·Product code JWH·April 30, 2026
BICONTACT PLASMAPORE 12/14 SIZE 17MM
FDA Adverse Event
Malfunction
·AESCULAP AG & CO. KG·Product code LWJ·April 27, 2012
AE-QAS-K521-53
FDA Adverse Event
Injury
·AESCULAP AG·Product code JWH·December 19, 2024
ENDURO
FDA Adverse Event
Injury
·AESCULAP AG·Product code JWH·November 14, 2024