BEUDAMED
    FDA Registration Active 🇺🇸 United States

    da Vinci Xi 12mm & Stapler Obturator, Blunt, Standard

    Reg #: 3015336263 · FEI: 3015336263 · Expires 2025
    View on FDA
    Products
    2
    Proprietary Names
    2
    Establishment Types
    1
    Classifications
    2

    Registration Details

    Registration Name
    SUPREME SCREW PRODUCTS
    Registration Number
    3015336263
    FEI Number
    3015336263
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    10 Skyline Dr
    City
    Plainview
    State
    NY
    ZIP
    11803
    Country
    US

    Regulatory Submissions

    510(k) Number
    K140553

    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
    Staple, Implantable GDW

    Proprietary Names

    da Vinci Xi 12mm & Stapler Obturator, Blunt, Standard da Vinci Xi 12mm & Stapler Obturator, Blunt, Long

    Establishment Types

    Manufacture Medical Device for Another Party (Contract Manufacturer)