BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Neulight®

    Reg #: 3007336385 · FEI: 3007336385 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    1
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    WEINERT Fiber Optics Inc.
    Registration Number
    3007336385
    FEI Number
    3007336385
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    209 Bulifants Blvd
    City
    Williamsburg
    State
    VA
    ZIP
    23188
    Country
    US

    Regulatory Submissions

    510(k) Number
    K201171

    Owner / Operator

    Firm Name
    WEINERT Fiber Optics, Inc.
    Operator Number
    10085607
    Address
    209 Bulifants Blvd.
    City
    Williamsburg
    State
    VA
    Postal Code
    23188
    Country
    US
    Correspondent
    Phillip LaCroix

    Products

    Device Name Product Code
    Powered Laser Surgical Instrument GEX

    Proprietary Names

    Neulight®

    Establishment Types

    Manufacture Medical Device