BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Kinetec Kooler Relief Pad Reusable

    Reg #: 3010675856 · FEI: 3010675856 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    2
    Establishment Types
    2
    Classifications
    1

    Registration Details

    Registration Name
    KINETEC USA
    Registration Number
    3010675856
    FEI Number
    3010675856
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    Yes
    Address
    N174W21475 Alcan Drive
    City
    Jackson
    State
    WI
    ZIP
    53037
    Country
    US

    Owner / Operator

    Firm Name
    Kinetec USA, Inc.
    Operator Number
    10045573
    Address
    N174W21475 Alcan Drive
    City
    Jackson
    State
    WI
    Postal Code
    53037
    Country
    US
    Correspondent
    Lori Kalsow

    Products

    Device Name Product Code
    Pack, Hot Or Cold, Reusable IME

    Proprietary Names

    Kinetec Kooler Relief Pad Reusable Dr. Aktive CCT

    Establishment Types

    Repack or Relabel Medical Device Develop Specifications But Do Not Manufacture At This Facility