BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Ventera®

    Reg #: 2031917 · FEI: 3002929183 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    2
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    CLASSIC WIRE CUT COMPANY, INC.
    Registration Number
    2031917
    FEI Number
    3002929183
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    28210 Constellation Rd
    City
    Valencia
    State
    CA
    ZIP
    91355
    Country
    US

    Regulatory Submissions

    510(k) Number
    K121351

    Owner / Operator

    Firm Name
    Classic Wire Cut Company, Inc.
    Operator Number
    9039170
    Address
    28210 Constellation Road, --
    City
    Valencia
    State
    CA
    Postal Code
    91355
    Country
    US
    Correspondent
    Marcy Martinez

    Products

    Device Name Product Code
    Instrument, Ent Manual Surgical LRC

    Proprietary Names

    Ventera® SINUS DILATION SYSTEM WITH CANNULATED INSTRUMENT

    Establishment Types

    Manufacture Medical Device for Another Party (Contract Manufacturer)