BEUDAMED
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    ANTEIS SA

    Manufacturer
    🇨🇭 Switzerland·1 Importer

    Ulthera Inc.

    Manufacturer
    🇺🇸 United States·1 Importer

    Merz North America, Inc.

    Manufacturer
    🇺🇸 United States·1 Importer

    MERZ AESTHETICS GMBH

    FDA registration
    MERZ AESTHETICS GMBH·1 product·🇩🇪 Germany

    MERZ AESTHETICS Dessau

    FDA registration
    MERZ AESTHETICS Dessau·1 product·🇩🇪 Germany

    RADIESSE DERMAL FILLER

    FDA Adverse Event
    Other ·MERZ AESTHETICS, INC.·Product code LMH·March 27, 2013

    RADIESSE DERMAL FILLER

    FDA Adverse Event
    Other ·MERZ AESTHETICS, INC.·Product code LMH·February 28, 2013

    MERZ AESTHETICS, 27G X 1.0 " (25MM) Cannula, Sterile R, QTY 20, Model 9015M1X20, Distributed by Merz Aesthetics, In., Manufactured by TSK Laboratory. The intended use of the Cannula is the injection of fluids into, or withdrawal of fluids from, parts of the body below the surface of the skin.

    FDA Recall
    Terminated ·Merz Aesthetics, Inc.·Product code FMI·December 16, 2011

    RADIESSE DERMAL FILLER

    FDA Adverse Event
    Other ·MERZ AESTHETICS, INC.·Product code LMH·January 13, 2012

    MERZ AESTHETICS, Radiesse Volume Advantage 1.5 CC, Injectable Implant, Part Number 8071M0H1 and 8071M0K1, Sterile, Rx ONLY. Part Number 8071M4K1 distributed in Canada Part Number 8071M5 distributed in Europe/Middle East/Africa Part Number 8071M9 distributed in Hong Kong, Korea, Malaysia.

    FDA Recall
    Terminated ·Merz Aesthetics, Inc.·Product code LMH·August 18, 2011

    Radiesse (+) Lidocaine, Injectable Implant 1.5cc, Rx only, P/N: 8063M0K1, Merz Aesthetics. Product Usage: RADIESSE is indicated for sub-dermal implantation for the correction of moderate to severe facial wrinkles and folds.

    FDA Enforcement
    Class II ·Terminated·Merz North America, Inc.·August 31, 2016

    RADIESSE DERMAL FILLER

    FDA Adverse Event
    Other ·MERZ AESTHETICS, INC.·Product code LMH·May 31, 2012

    RADIESSE DERMAL FILLER

    FDA Adverse Event
    Other ·MERZ AESTHETICS, INC.·Product code LMH·July 20, 2012

    RADIESSE DERMAL FILLER

    FDA Adverse Event
    Other ·MERZ AESTHETICS, INC.·Product code LMH·July 20, 2012

    RADIESSE DERMAL FILLER

    FDA Adverse Event
    Other ·MERZ AESTHETICS, INC.·Product code LMH·March 22, 2013

    RADIESSE DERMAL FILLER

    FDA Adverse Event
    Injury ·Product code LMH·June 15, 2011

    RADIESSE(+)

    FDA Adverse Event
    Injury ·MERZ NORTH AMERICA, INC (FRANKSVILLE)·Product code LMH·December 15, 2025

    Radiesse (+) Lidocaine, Injectable Implant 1.5cc, Rx only, P/N: 8063M0K1, Merz Aesthetics. Product Usage: RADIESSE is indicated for sub-dermal implantation for the correction of moderate to severe facial wrinkles and folds.

    FDA Recall
    Terminated ·Merz North America, Inc.·Product code LMH·May 20, 2016

    RADIESSE, VOLUMIZING FILLER

    FDA Adverse Event
    Injury ·MERZ AESTHETICS·Product code LMH·August 27, 2013

    RADIESSE DERMAL FILLER

    FDA Adverse Event
    Other ·MERZ AESTHETICS, INC.·Product code LMH·April 18, 2013