BEUDAMED
    FDA PMA FDA Class 3 Approved 🇺🇸 United States

    Implant, Dermal, For Aesthetic Use

    PMA: P040024 · Supplement: S073 · Decision Jul 1, 2015
    View on FDA
    Classifications
    1
    FEI Numbers
    29
    Registration Numbers
    29

    Basic Information

    Device Name
    Implant, Dermal, For Aesthetic Use
    Trade Name
    RESTYLANE, RESTYLANE-L,PERLANE,PERLANE-L,RESTYLANE SILK
    PMA Number
    P040024
    Supplement Number
    S073
    Device Class
    FDA Class 3
    Product Code
    LMH
    Generic Name
    Implant, dermal, for aesthetic use
    Medical Specialty
    Unknown
    Advisory Committee
    General, Plastic Surgery
    Decision
    Approved
    Decision Code
    APPR
    Decision Date
    July 1, 2015
    Date Received
    May 1, 2014
    Supplement Type
    Panel Track
    Supplement Reason
    Labeling Change - Indications/instructions/shelf life/tradename
    Expedited Review
    N
    Docket Number
    15M-2634

    Advisory Committee Statement

    APPROVAL FOR RESTYLANE LYFT WITH LIDOCAINE. THIS DEVICE IS INDICATED FOR IMPLANTATION INTO THE DEEP DERMIS TO SUPERFICIAL SUBCUTIS FOR THE CORRECTION OF MODERATE TO SEVERE FACIAL FOLDS AND WRINKLES, SUCH AS NASOLABIAL FOLDS; AND FOR SUBCUTANEOUS TO SUPRAPERIOSTEAL IMPLANTATION FOR CHEEK AUGMENTATION AND CORRECTION OF AGE-RELATED MIDFACE CONTOUR DEFICIENCIES IN PATIENTS OVER THE AGE OF 21.

    Classifications

    This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    LMH Implant, Dermal, For Aesthetic Use