114 results · 24ms · Sources: EU EUDAMED, US FDA

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Reform Pedicle Screw System

FDA 510(k)
FDA Class 2 ·Orthopedic

HHM

FDA UDI
Oticon A/S·05707131282200·H160V2 TI, BTE 13 WL 85 CBE HHM

BIOMET KNEE SYSTEM

FDA UDI
Biomet Orthopedics, LLC·00880304207950·

Biomet® Knee System

FDA UDI
Biomet Orthopedics, LLC·00887868241635·

LCG (LIQUIDE CRYSTAL GLASSES) SYSTEM

FDA 510(k)
FDA Class 1 ·Ophthalmic

POWDERED VINYL PATIENT EXAMINATION GLOVES, CLEAR (NON-COLORED)

FDA 510(k)
FDA Class 1 ·General Hospital

BIOMET BONE CEMENT R 40X2

FDA Adverse Event
Malfunction ·BIOMET FRANCE S.A.R.L.·Product code MBB·November 9, 2016

BIOMET BONE CEMENT V

FDA Adverse Event
Injury ·BIOMET FRANCE S.A.R.L.·Product code MBB·December 1, 2016

BIOMET BONE CEMENT V

FDA Adverse Event
Injury ·BIOMET FRANCE S.A.R.L.·Product code MBB·December 1, 2016

OPTIPAC-S 60 REFOBACIN BONE CEMENT R

FDA Adverse Event
Malfunction ·BIOMET FRANCE S.A.R.L.·Product code MBB·June 14, 2016

REFOBACIN BONE CEMENT R 2X40G

FDA Adverse Event
Malfunction ·BIOMET FRANCE S.A.R.L.·Product code MBB·February 2, 2018

OPTIPAC-S KNEE REFOBACIN PLUS BONE CEMNT

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

BIOMET BONE CEMENT 1X40G

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

BIOMET BONE CEMENT R 2X40G

FDA Adverse Event
Malfunction ·BIOMET FRANCE S.A.R.L.·Product code MBB·July 9, 2016

OPTIPAC-S 60 REFOBACIN BONE CEMENT R

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

OPTIPAC-S 40 REFOBACIN PLUS BONE CEMENT

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

OPTIPAC-S 40 REFOBACIN PLUS BONE CEMENT

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

BIOMET BONE CEMENT V

FDA Adverse Event
Injury ·BIOMET FRANCE S.A.R.L.·Product code MBB·December 1, 2016

BIOMET BONE CEMENT 1X40G

FDA Adverse Event
Malfunction ·BIOMET FRANCE S.A.R.L.·Product code MBB·July 20, 2016

BIOMET BONE CEMENT R 40

FDA Adverse Event
Malfunction ·BIOMET FRANCE S.A.R.L.·Product code MBB·September 30, 2016