283 results · 28ms · Sources: EU EUDAMED, US FDA

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EBI, L.P.'S LINE EXTENSION TO THE ARRAY SPINAL SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

EBICE COLD THERAPY

FDA Adverse Event
Injury ·EBI, L.P.·Product code ILO·February 6, 2009

INTERGRO

FDA Adverse Event
Injury ·EBI, L.P.·Product code MQV·March 26, 2009

ARRAY SPINAL SYSTEM

FDA Adverse Event
Malfunction ·EBI, L.P.·Product code MNI·January 21, 2009

VUELOCK IMPLANTS

FDA Adverse Event
Malfunction ·EBI, L.P.·Product code KWQ·March 6, 2009

T30 PROVISIONAL DRIVER

FDA Adverse Event
Malfunction ·EBI, L.P.·Product code HXX·March 6, 2009

ARRAY TITATNIUM IMPLANTS, SCREW

FDA Adverse Event
Injury ·EBI, L.P.·Product code MNI·March 31, 2009

SPINAL LUMBAR IMPLANTS

FDA Adverse Event
Malfunction ·EBI, L.P.·Product code KWQ·March 16, 2009

C-TEK MAXAN IMPLANTS

FDA Adverse Event
Malfunction ·EBI, L.P.·Product code KWQ·March 6, 2009

SPINELINK

FDA Adverse Event
Malfunction ·EBI, L.P.·Product code KWQ·March 7, 2002

EBI XFIX DYNAFIX

FDA Adverse Event
Injury ·EBI, L.P.·Product code JEC·March 7, 2002

SPINELINK

FDA Adverse Event
Malfunction ·EBI, L.P.·Product code KWQ·March 7, 2002

EBI XFIX DYNAFIX

FDA Adverse Event
Injury ·EBI, L.P.·Product code HTY·November 6, 2003

OMEGA-21 SYSTEM

FDA Adverse Event
Malfunction ·EBI, L.P.·Product code JDN·November 10, 2003

EBI

FDA Adverse Event
Other ·EBI, L.P.·Product code JDN·October 30, 2003

SPINELINK II

FDA Adverse Event
Malfunction ·EBI, L.P.·Product code KWQ·November 4, 2003

OMEGA-21 SYSTEM

FDA Adverse Event
Malfunction ·EBI, L.P.·Product code JDN·October 22, 2003

EBI XFIX DYNAFIX

FDA Adverse Event
Malfunction ·EBI, L.P.·Product code KTT·November 6, 2003

SPINELINK II

FDA Adverse Event
Malfunction ·EBI, L.P.·Product code JDN·October 22, 2003

EBI XFIX DYNAFIX

FDA Adverse Event
Malfunction ·EBI, L.P.·Product code KTT·November 6, 2003