10,000 results · 58ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

TI MATRIXNEURO SCREW SELF-DRILLING 4MM

FDA Adverse Event
Injury ·SYNTHES USA·Product code JEY·May 8, 2013

UNKNOWN PRE-CONTOURED MESH

FDA Adverse Event
Injury ·BIOMET MICROFIXATION·Product code GXN·October 13, 2016

PSI SD800.418 PEEK IMPLANT

FDA Adverse Event
Injury ·SYNTHES BRANDYWINE·Product code GXN·November 23, 2016

HTR-PEKK

FDA Adverse Event
OXFORD PERFORMANCE MATERIALS, INC.·Product code GXN·August 7, 2015

PSI SD800.540 PEEK IMPLANT

FDA Adverse Event
Injury ·SYNTHES BRANDYWINE·Product code GXN·August 25, 2015

STRYKER CMF

FDA Adverse Event
Malfunction ·Product code GXN·January 13, 2009

PATIENT SPECIFIC IMPLANT

FDA Adverse Event
Injury ·SYNTHES BRANDYWINE·Product code GXN·February 6, 2009

LEIBINGER PRIMARY RECONSTRUCTION PLATE

FDA Adverse Event
Injury ·STRYKER CRANIOMAXILLFACIAL·Product code GXN·January 27, 2009

HTR-PEKK

FDA Adverse Event
Injury ·OXFORD PERFORMANCE MATERIALS·Product code GXN·April 14, 2014

PSI SD800.418

FDA Adverse Event
Injury ·SYNTHES BRANDYWINE·Product code GXN·April 10, 2014

PSI SD800.441 PEEK IMPLANT

FDA Adverse Event
Injury ·SYNTHES BRANDYWINE·Product code GXN·June 13, 2014

HTR-PEKK

FDA Adverse Event
OXFORD PERFORMANCE MATERIALS·Product code GXN·June 16, 2014

TI CRANIAL FLAP TUBE CLAMP 13MM DIA

FDA Adverse Event
Malfunction ·SYNTHES (USA)·Product code GXN·June 26, 2014

PSI SD800.430 PEEK IMPLANT

FDA Adverse Event
Malfunction ·SYNTHES BRANDYWINE·Product code GXN·June 5, 2014

HTR-PMI

FDA Adverse Event
Injury ·BIOMET MICROFIXATION·Product code GXN·June 3, 2014

PSI SD800.419 PEEK IMPLANT

FDA Adverse Event
Malfunction ·SYNTHES MEZZOVICO·Product code GXN·April 21, 2014

PSI SD800.402 PEEK IMPLANT

FDA Adverse Event
Injury ·SYNTHES MEZZOVICO·Product code GXN·April 23, 2014

PSI SD800.411

FDA Adverse Event
Injury ·SYNTHES BRANDYWINE·Product code GXN·April 10, 2014

MEDPOR IMPLANT

FDA Adverse Event
Injury ·POREX SURGICAL, INC.·Product code GXN·February 25, 2010

MEDPOR IMPLANT

FDA Adverse Event
Injury ·POREX SURGICAL·Product code GXN·January 25, 2010