BEUDAMED
    FDA Registration Active 🇺🇸 United States

    SUPREME SCREW PRODUCTS

    Reg #: 3015336263 · FEI: 3015336263 · Expires 2026
    View on FDA
    Products
    4
    Proprietary Names
    13
    Establishment Types
    2
    Classifications
    4

    Registration Details

    Registration Name
    SUPREME SCREW PRODUCTS
    Registration Number
    3015336263
    FEI Number
    3015336263
    Status
    Active
    Expiry Year
    2026
    Initial Importer
    No
    Address
    10 Skyline Dr
    City
    Plainview
    State
    NY
    ZIP
    11803
    Country
    US

    Owner / Operator

    Firm Name
    Supreme Screw Products
    Operator Number
    10081122
    Address
    10 Skyline Dr
    City
    Plainview
    State
    NY
    Postal Code
    11803
    Country
    US
    Correspondent
    Nicole Needle

    Products

    Device Name Product Code
    System, Surgical, Computer Controlled Instrument NAY
    Laparoscope, General & Plastic Surgery GCJ
    Staple, Implantable GDW
    Sterilization Wrap Containers, Trays, Cassettes & Other Accessories KCT

    Proprietary Names

    da Vinci Xi 12mm & Stapler Bladeless Obturator, Long da Vinci Xi 12mm & Stapler Bladeless, Obturator, Standard da Vinci Xi 12mm & Stapler Obturator, Blunt, Standard da Vinci Xi 12mm & Stapler Obturator, Blunt, Long da Vinci Xi Gage Pin da Vinci Xi 8 mm Blunt Obturator da Vinci Xi 8 mm Blunt Obturator Long SP Reprocessing Connector, 1 device SP Reprocessing Connector, 2 device da Vinci S, Si 8mm Blunt Obturator da Vinci Xi 12mm & Stapler Hasson Cone da Vinci Xi 8 mm Hasson Cone da Vinci Xi 5 mm Obturator

    Establishment Types

    Manufacture Medical Device for Another Party (Contract Manufacturer) Manufacture Device in the United States for Export Only