BEUDAMED
    37 results · 33ms · Sources: EU EUDAMED, US FDA

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    PROGENIX DBM PUTTY AND PASTE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BRIDGE III RECEIVER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MODIFICATION TO MARSPO2, MODEL 2001

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    LINEAR ST

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·October 11, 2018

    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

    TFNA HELICAL BLADE 90MM

    FDA Adverse Event
    Injury ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HSB·July 23, 2019

    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

    OBTRYX SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·April 16, 2013

    SILICONE ADVANCED OPTIC-VIOLET SHIELD

    FDA Adverse Event
    Malfunction ·BAUSCH & LOMB·Product code HQL·June 12, 2008

    ULTRACISION HARMONIC ACE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·April 18, 2011

    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