BEUDAMED
    FDA Registration Active 🇺🇸 United States

    VESTA

    Reg #: 2182291 · FEI: 2182291 · Expires 2026
    View on FDA
    Products
    10
    Proprietary Names
    7
    Establishment Types
    1
    Classifications
    10

    Registration Details

    Registration Name
    VESTA
    Registration Number
    2182291
    FEI Number
    2182291
    Status
    Active
    Expiry Year
    2026
    Initial Importer
    No
    Address
    9900 S 57th St
    City
    Franklin
    State
    WI
    ZIP
    53132
    Country
    US

    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
    Stimulator, Spinal-Cord, Totally Implanted For Pain Relief LGW
    Stimulator, Spinal-Cord, Totally Implanted For Relief Of Pain Due To Diabetic Neuropathy QRB
    Tubes, Gastrointestinal (And Accessories) KNT
    Orthopedic Manual Surgical Instrument LXH
    Instrument, Manual, Surgical, General Use MDM
    Surgical Device, For Cutting, Coagulation, And/Or Ablation Of Tissue, Including Cardiac Tissue OCL
    Instrument, Ultrasonic Surgical LFL
    Electrosurgical, Cutting & Coagulation & Accessories GEI
    Surgical Cardiac Ablation Device, For Treatment Of Atrial Fibrillation OCM
    Apparatus, Suction, Single Patient Use, Portable, Nonpowered GCY

    Proprietary Names

    Boston Scientific - 32 Contact Long Paddle Blank (VPN 26210) Boston Scientific - 32 Contact Short Paddle Blank (VPN 26209) Gastrointestinal Boundary Identifier (GIBI HD) Subtle® Cannula with Guide, 30cm Subtle® Cannula LAP-BAND System Calibration Tube INTERI MANIFOLD

    Establishment Types

    Manufacture Medical Device for Another Party (Contract Manufacturer)