BEUDAMED
    FDA Registration Active 🇺🇸 United States

    LAP-BAND System Calibration Tube

    Reg #: 2182291 · FEI: 2182291 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    1
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    VESTA
    Registration Number
    2182291
    FEI Number
    2182291
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    9900 S 57th St
    City
    Franklin
    State
    WI
    ZIP
    53132
    Country
    US

    Regulatory Submissions

    510(k) Number
    K220455

    Owner / Operator

    Firm Name
    Vesta
    Operator Number
    10043140
    Address
    9900 S 57th St
    City
    Franklin
    State
    WI
    Postal Code
    53132
    Country
    US
    Correspondent
    Christopher Kobus

    Products

    Device Name Product Code
    Tubes, Gastrointestinal (And Accessories) KNT

    Proprietary Names

    LAP-BAND System Calibration Tube

    Establishment Types

    Manufacture Medical Device for Another Party (Contract Manufacturer)