BEUDAMED
    FDA Registration Active 🇺🇸 United States

    TEK-CLEAR Accommodative IOLs Model 500 Series

    Reg #: 2031474 · FEI: 3002023310 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    5
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    TEKIA, INC.
    Registration Number
    2031474
    FEI Number
    3002023310
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    17 Hammond, suite 414
    City
    Irvine
    State
    CA
    ZIP
    92618
    Country
    US

    Owner / Operator

    Firm Name
    TEKIA, INC
    Operator Number
    10023535
    Address
    17 Hammond, suite 414
    City
    Irvine
    State
    CA
    Postal Code
    92618
    Country
    US
    Correspondent
    gene currie

    Products

    Device Name Product Code
    Intraocular Lens HQL

    Proprietary Names

    TEK-CLEAR Accommodative IOLs Model 500 Series TEKLENS II Three Piece Hydrophlic Acrylic IOLs Model 600 & 600Y Series TEKTOR Single Piece Acrylic Toric IOLs Model 820 &820Y TEKLENS II Single Piece Hydrophlic Acrylic IOLs Model 800 & 800Y Series TEKLENS III Hydrophobic Acrylic IOLs Model 900 series

    Establishment Types

    Manufacture Device in the United States for Export Only