BEUDAMED
    9 results · 28ms · 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.
    Filters Status: Injury ×

    INDURA

    FDA Adverse Event
    Injury ·RICE CREEK MANUFACTURING·Product code LKK·May 7, 2008

    ENDOTAK RELIANCE

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVY·April 5, 2011

    RESTYLANE, RESTYLANE

    FDA Adverse Event
    Injury ·Q-MED·Product code LMH·June 11, 2013

    RESTYLANE INJECTABLE GEL

    FDA Adverse Event
    Injury ·Q-MED AB·Product code LMH·August 26, 2011

    AFX

    FDA Adverse Event
    Injury ·ENDOLOGIX INC.·Product code MIH·March 1, 2017

    RESTYLANE, RESTYLANE

    FDA Adverse Event
    Injury ·Q-MED·Product code LMH·July 11, 2013

    RESTYLANE PERLANE

    FDA Adverse Event
    Injury ·GALDERMA Q-MED·Product code LMH·April 24, 2015

    RESTYLANE, RESTYLANE

    FDA Adverse Event
    Injury ·Q-MED·Product code LMH·February 14, 2014

    RESTYLANE, RESTYLANE

    FDA Adverse Event
    Injury ·Q-MED·Product code LMH·February 21, 2014