1,319 results · 70ms · Sources: EU EUDAMED, US FDA

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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