BEUDAMED
    FDA Registration Active 🇺🇸 United States

    POLO CUSTOM PRODUCTS

    Reg #: 3016704581 · FEI: 3016704581 · Expires 2026
    View on FDA
    Products
    2
    Proprietary Names
    2
    Establishment Types
    1
    Classifications
    2

    Registration Details

    Registration Name
    POLO CUSTOM PRODUCTS
    Registration Number
    3016704581
    FEI Number
    3016704581
    Status
    Active
    Expiry Year
    2026
    Initial Importer
    No
    Address
    15730 W Main Street
    City
    Louisville
    State
    MS
    ZIP
    39339
    Country
    US

    Owner / Operator

    Firm Name
    Polo Custom Products
    Operator Number
    9919026
    Address
    3601 SW 29th Street, --
    City
    Topeka
    State
    KS
    Postal Code
    66614
    Country
    US
    Correspondent
    Dawn R Silver

    Products

    Device Name Product Code
    Prep Kit PXD
    Clamp, Vascular DXC

    Proprietary Names

    Emergency Kit Abdominal Aortic and Junctional Tourniquet - Stabilized (AAJT-S)

    Establishment Types

    Manufacture Medical Device for Another Party (Contract Manufacturer)