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

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    Filters Status: Injury ×

    RADIESSE

    FDA Adverse Event
    Injury ·BIOFORM MEDICAL, INC.·Product code LMH·December 15, 2007

    RADIESSE DERMAL FILLERS

    FDA Adverse Event
    Injury ·MERZ NORTH AMERICA, INC.·Product code LMH·February 29, 2024

    RADIESSE DERMAL FILLERS

    FDA Adverse Event
    Injury ·MERZ NORTH AMERICA, INC.·Product code LMH·February 29, 2024

    RADIESSE DERMAL FILLERS

    FDA Adverse Event
    Injury ·MERZ NORTH AMERICA, INC.·Product code LMH·February 29, 2024

    SCULPTRA

    FDA Adverse Event
    Injury ·GALDERMA LABORATORIES, L.P.·Product code LMH·July 29, 2024

    COOLSCULPTING

    FDA Adverse Event
    Injury ·ALLERGAN / ZELTIQ AESTHETICS INC.·Product code OOK·February 2, 2024

    BELLAFILL

    FDA Adverse Event
    Injury ·SUNEVA·Product code LMH·January 28, 2016

    OUTER TUBE

    FDA Adverse Event
    Injury ·AB MEDICA SAS·Product code GCJ·March 23, 2020

    MICROLAP CRVD SCISSORS INSERT

    FDA Adverse Event
    Injury ·AB MEDICA SAS·Product code GCJ·August 27, 2019

    BELOTERO

    FDA Adverse Event
    Injury ·MERZ NORTH AMERICA, INC.·Product code LMH·May 1, 2019

    HYDROGEL

    FDA Adverse Event
    Injury ·UNK·Product code PFP·November 24, 2020

    MORPHEUS 8 RADIO FREQUENCY DEVICE

    FDA Adverse Event
    Injury ·INMODE LTD.·Product code GEI·October 21, 2025

    SYLFIRM X

    FDA Adverse Event
    Injury ·BENEV / VIOL CO., LTD.·Product code GEI·June 13, 2023

    LIGHTSHEER (ALL MODELS)

    FDA Adverse Event
    Injury ·RH-USA·Product code GEX·November 2, 2007

    RADIESSE INJECTABLE IMPLANT

    FDA Adverse Event
    Injury ·MERZ NORTH AMERICA, INC.·Product code LMH·March 20, 2019

    IONIXLIGHT (OR OXYLIGHT)

    FDA Adverse Event
    Injury ·RAJA TRADING COMPANY, INC.·Product code NFO·October 6, 2020

    FACE FILLER

    FDA Adverse Event
    Injury ·UNK·Product code LMH·April 28, 2023

    LUMENIS M22

    FDA Adverse Event
    Injury ·LUMENIS AESTHETIC·Product code GEX·October 30, 2013

    FRAXEL RESTORE

    FDA Adverse Event
    Injury ·Product code GEX·April 24, 2015

    BAREIT LASER

    FDA Adverse Event
    Injury ·SCITON, INC.·Product code GEX·December 11, 2024