BEUDAMED
    FDA Registration Active 🇺🇸 United States

    MediShield

    Reg #: 2031637 · FEI: 3004474407 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    6
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    FZIOMED, INC.
    Registration Number
    2031637
    FEI Number
    3004474407
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    231 BONETTI DR
    City
    San Luis Obispo
    State
    CA
    ZIP
    93401
    Country
    US

    Owner / Operator

    Firm Name
    FZIOMED, INC.
    Operator Number
    9034681
    Address
    231 BONETTI DR., --
    City
    San Luis Obispo
    State
    CA
    Postal Code
    93401
    Country
    US
    Correspondent
    Lisa S Gawehn

    Products

    Device Name Product Code
    Inhibitor, Peridural Fibrosis (Adhesion Barrier) MLQ

    Proprietary Names

    MediShield Interpose Oxiplex 1mL Oxiplex/SP Gel Oxiplex MediShield 1mL

    Establishment Types

    Manufacture Device in the United States for Export Only