BEUDAMED
    FDA PMA FDA Class 3 Approved 🇺🇸 United States

    Intraocular Lens

    PMA: P930014 · Supplement: S154 · Decision Mar 21, 2025
    View on FDA
    Classifications
    1
    FEI Numbers
    59
    Registration Numbers
    59

    Basic Information

    Device Name
    Intraocular Lens
    Trade Name
    AcrySof Posterior Chamber Intraocular Lenses
    PMA Number
    P930014
    Supplement Number
    S154
    Device Class
    FDA Class 3
    Product Code
    HQL
    Generic Name
    intraocular lens
    Regulation Number
    886.3600
    Medical Specialty
    Ophthalmic
    Advisory Committee
    Ophthalmic
    Decision
    Approved
    Decision Code
    APPR
    Decision Date
    March 21, 2025
    Date Received
    January 21, 2025
    Supplement Type
    Normal 180 Day Track No User Fee
    Supplement Reason
    Location Change - Manufacturer/Sterilizer/Packager/Supplier
    Expedited Review
    N

    Advisory Committee Statement

    approval for a manufacturing site, PT. Ciba Vision Batam, located at Jalan Beringin Lot #204, Batamindo Industrial Park, Mukakuning, Batam Island 29433, Indonesia. This site will perform manufacturing and sterilization of the AcrySof single-piece intraocular lens - models SN60WF, SN60AT, SA60WF AND SA60AT

    Classifications

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

    Product Code Device Name
    HQL Intraocular Lens