BEUDAMED
    FDA Registration Active 🇺🇸 United States

    HDX 2-Way Silicone Foley Catheter

    Reg #: 3014650073 · FEI: 3014650073 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    1
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    Silq Technologies Corporation
    Registration Number
    3014650073
    FEI Number
    3014650073
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    323 Sunny Isles Blvd., 7th Floor
    City
    Sunny Isles Beach
    State
    FL
    ZIP
    33160
    Country
    US

    Regulatory Submissions

    510(k) Number
    K192034

    Owner / Operator

    Firm Name
    Silq Technologies Corporation
    Operator Number
    10077941
    Address
    323 Sunny Isles Blvd., 7th Floor
    City
    Sunny Isles Beach
    State
    FL
    Postal Code
    33160
    Country
    US
    Correspondent
    D. Verne Sharma

    Products

    Device Name Product Code
    Catheter, Retention Type, Balloon EZL

    Proprietary Names

    HDX 2-Way Silicone Foley Catheter

    Establishment Types

    Manufacture Medical Device