BEUDAMED
    FDA Registration Active 🇩🇪 Germany

    Light, Fiberoptic, Dental

    Reg #: 3006984721 · FEI: 3006984721 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    2
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    SCHOTT AG
    Registration Number
    3006984721
    FEI Number
    3006984721
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    Otto Schott Strasse 2
    City
    Mainz Rhineland-Palatinate
    Country
    DE

    Regulatory Submissions

    510(k) Number
    K071251

    Owner / Operator

    Firm Name
    SCHOTT AG
    Operator Number
    10025267
    Address
    Hattenbergstrasse 10
    City
    Mainz
    State
    Rhineland-Palatinate
    Postal Code
    55122
    Country
    DE
    Correspondent
    Todd L Peloquin

    US Agent

    Business Name
    SCHOTT North America Inc, - Lighting and Imaging
    Contact Name
    Todd Peloquin
    Address
    122 Charlton St.
    City
    Southbridge
    State
    MA
    ZIP
    01550
    Country
    US
    Email
    [email protected]
    Phone
    508 7653279

    Products

    Device Name Product Code
    Activator, Ultraviolet, For Polymerization EBZ

    Proprietary Names

    Light, Fiberoptic, Dental Fiber Optic Rod

    Establishment Types

    Manufacture Medical Device for Another Party (Contract Manufacturer)