BEUDAMED
    FDA PMA FDA Class 3 30-Day Notice Accepted 🇺🇸 United States

    Lens, Multifocal Intraocular

    PMA: P080010 · Supplement: S025 · Decision Jun 17, 2024
    View on FDA
    Classifications
    1
    FEI Numbers
    18
    Registration Numbers
    18

    Basic Information

    Device Name
    Lens, Multifocal Intraocular
    Trade Name
    TECNIS® Multifocal 3-Piece IOL, Model ZMA00
    PMA Number
    P080010
    Supplement Number
    S025
    Device Class
    FDA Class 3
    Product Code
    MFK
    Generic Name
    Lens, multifocal intraocular
    Regulation Number
    886.3600
    Medical Specialty
    Ophthalmic
    Advisory Committee
    Ophthalmic
    Decision
    30-Day Notice Accepted
    Decision Code
    OK30
    Decision Date
    June 17, 2024
    Date Received
    May 29, 2024
    Supplement Type
    30-Day Notice
    Supplement Reason
    Process Change - Manufacturer/Sterilizer/Packager/Supplier
    Expedited Review
    N

    Advisory Committee Statement

    add a new haptic-loop inspection vision system to the production process of the SENSAR® Soft Acrylic Posterior Chamber IOL, Models AR40e, AR40E, and AR40M, TECNIS® Foldable Acrylic IOL with OptiEdge, ZA9003, and TECNIS® Multifocal 3-PC, Model ZMA00 IOLs at the JJSV Añasco, Puerto Rico manufacturing site

    Classifications

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

    Product Code Device Name
    MFK Lens, Multifocal Intraocular