BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Difiney Advanced Anti Snoring Device 4

    Reg #: 3031978086 · FEI: 3031978086 · Expires 2025
    View on FDA
    Products
    2
    Proprietary Names
    1
    Establishment Types
    1
    Classifications
    2

    Registration Details

    Registration Name
    FISSIONTECH LLC
    Registration Number
    3031978086
    FEI Number
    3031978086
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    1 Liberty Plz Fl 3
    City
    New York
    State
    NY
    ZIP
    10006
    Country
    US

    Regulatory Submissions

    510(k) Number
    K250482

    Owner / Operator

    Firm Name
    Fissiontech LLC
    Operator Number
    10091230
    Address
    1 Liberty Plz FL 3
    City
    New York
    State
    NY
    Postal Code
    10006
    Country
    US
    Correspondent
    Mike Lee

    Products

    Device Name Product Code
    Device, Anti-Snoring LRK
    Device, Jaw Repositioning LQZ

    Proprietary Names

    Difiney Advanced Anti Snoring Device 4

    Establishment Types

    Manufacture Medical Device