37 results · 19ms · Sources: EU EUDAMED, US FDA

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TRABECULAR METAL VERTEBRAL BODY REPLACEMENT, MODEL 06-165-011X1 AND 06-166-051X1

FDA 510(k)
FDA Class 2 ·Orthopedic

JEL BIOS 90 (CODE NAME RD-2401)

FDA 510(k)
FDA Class 2 ·Dental

IQUANTIFY, VERSION 1.0

FDA 510(k)
FDA Class 2 ·Radiology

COBALT HV BN CMT 40G-JAPAN

FDA Adverse Event
Malfunction ·BIOMET ORTHOPEDICS·Product code LOD·July 29, 2016

REFOBACIN PLUS BONE CEMENT 40

FDA Adverse Event
Death ·BIOMET FRANCE S.A.R.L·Product code LOD·December 3, 2015

MARKERS

FDA Adverse Event
Malfunction ·PRAXIM·Product code HAW·January 3, 2007

REFOBACIN BONE CEMENT R 40X2 GERMAN

FDA Adverse Event
Injury ·BIOMET FRANCE S.A.R.L·Product code LOD·November 23, 2015

OPTIPAC-S 40 REFOBACIN BONE CEMENT R

FDA Adverse Event
Malfunction ·BIOMET FRANCE S.A.R.L.·Product code MBB·March 22, 2016

OPTIPAC-S 60 REFOBACIN BONE CEMENT R

FDA Adverse Event
Malfunction ·BIOMET FRANCE S.A.R.L.·Product code MBB·March 23, 2016

OPTIPAC SOFTPAC HIPSET

FDA Adverse Event
Malfunction ·BIOMET FRANCE S.A.R.L.·Product code MBB·March 17, 2016

OPTIPAC-S 60 REFOBACIN BONE CEMENT R

FDA Adverse Event
Malfunction ·BIOMET FRANCE S.A.R.L.·Product code LOD·October 25, 2016

OPTIPAC-S 60 REFOB BN CMT R

FDA Adverse Event
Malfunction ·BIOMET FRANCE S.A.R.L.·Product code LOD·October 25, 2016

OPTIPAC-S 40 REFOBACIN BONE CEMENT R

FDA Adverse Event
Malfunction ·BIOMET FRANCE S.A.R.L.·Product code MBB·March 23, 2016

OPTIPAC-S 40 REFOBACIN BONE CEMENT R

FDA Adverse Event
Malfunction ·BIOMET FRANCE S.A.R.L.·Product code MBB·March 17, 2016

OPTIPAC-S 80 REFOBACIN BONE CEMENT R

FDA Adverse Event
Malfunction ·BIOMET FRANCE S.A.R.L.·Product code MBB·March 17, 2016

OPTIPAC-S 60 REFOBACIN BONE CEMENT R

FDA Adverse Event
Malfunction ·BIOMET FRANCE S.A.R.L.·Product code MBB·April 6, 2016

OPTIPAC-S 40 REFOBACIN BONE CEMENT R

FDA Adverse Event
Malfunction ·BIOMET FRANCE S.A.R.L.·Product code MBB·April 7, 2016

OPTIPAC-S 80 REFOBACIN PLUS BONE CEMENT

FDA Adverse Event
Malfunction ·BIOMET FRANCE S.A.R.L.·Product code MBB·April 5, 2016

PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE

FDA Adverse Event
Injury ·MPRI·Product code LWP·April 10, 2013

CAPSURE EPI

FDA Adverse Event
Injury ·MEDTRONIC, INC.·Product code DTB·April 12, 2011