BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Fibreplast

    Reg #: 2247992 · FEI: 1000208827 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    6
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    Anholt Technologies Inc.
    Registration Number
    2247992
    FEI Number
    1000208827
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    Yes
    Address
    440 CHURCH ROAD
    City
    Avondale
    State
    PA
    ZIP
    19311
    Country
    US

    Regulatory Submissions

    510(k) Number
    K935067

    Owner / Operator

    Firm Name
    Medtec LLC
    Operator Number
    9033077
    Address
    1401 8TH ST., S.E., --
    City
    Orange City
    State
    IA
    Postal Code
    51041
    Country
    US

    Products

    Device Name Product Code
    Accelerator, Linear, Medical IYE

    Proprietary Names

    Fibreplast VariablePerf Assure Integrity Series IntegraBite Aquaplast

    Establishment Types

    Manufacture Medical Device