BEUDAMED
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    NEX-LINK SPINAL FIXATION SYSTEM ROD TO ROD CONNECTORS, MODELS 725, 726 SERIES

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Mini-Mono®

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR70606341·Mini-Mono-Brackets Roth 'S2' .022" 9° 400 Brack...

    HEARTSTREAM XL DEFIBIBRILLATOR/MONITOR, MODEL M4735A, HEARTSTREAM XLT DEFIBRILLATOR/MONITOR.MODEL M2500B

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    ROD TO ROD CROSS BRACES

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    TESS HUM INSERT TH 6 DIA36 S1

    FDA Adverse Event
    Malfunction ·BIOMET FRANCE S.A.R.L.·Product code KWS·March 7, 2017

    TESS HUMERAL INSERT TH 8 DIA36 S0

    FDA Adverse Event
    Malfunction ·BIOMET FRANCE S.A.R.L.·Product code KWS·February 15, 2017

    TESS HUMERAL REVERSED INLAY 036 S1 12MM

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code KWS·February 9, 2017

    TESS HUMERAL INSERT TH 6 DIA36 S0

    FDA Adverse Event
    Malfunction ·BIOMET FRANCE S.A.R.L.·Product code KWS·February 15, 2017

    CUSTOM REVERSE HUMERAL LINER

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code KWS·February 27, 2017

    TESS GLEN BASEPLATE S0

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

    TESS HUMERAL REVERSE COROLLA S0

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code KWS·November 18, 2016

    UNKNOWN TESS GLENOID COMPONENT

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code KWS·July 7, 2017

    TESS HUM INSERT TH 6 DIA36 S0

    FDA Adverse Event
    Malfunction ·BIOMET FRANCE S.A.R.L.·Product code KWS·May 10, 2017

    UNKNOWN TESS HUMERAL INSERT

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code KWS·June 1, 2017

    DEPUY ASR XL FEM IMP SIZE 49

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·April 16, 2013

    ENDURON NEUT 52OD X 28ID

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code KWY·April 6, 2011

    UNK

    FDA Adverse Event
    Injury ·Product code FWM·June 10, 2008

    TESS HUMERAL INSERT TH 8 DIA36 S0

    FDA Adverse Event
    Malfunction ·BIOMET FRANCE S.A.R.L.·Product code KWS·February 17, 2017

    TESS HUMERAL INSERT TH 6 DIA36 S0

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code KWS·January 25, 2017

    TESS HUM INSERT TH 6 DIA36 S0

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code KWS·February 6, 2017