BEUDAMED
    FDA Registration Active 🇺🇸 United States

    TELIGEN Procedure Kit Pro

    Reg #: 1221485 · FEI: 1221485 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    3
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    Viant AS&O Holdings, LLC
    Registration Number
    1221485
    FEI Number
    1221485
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    45 Lexington Dr
    City
    LACONIA
    State
    NH
    ZIP
    03246
    Country
    US

    Regulatory Submissions

    510(k) Number
    K233254

    Owner / Operator

    Firm Name
    Viant Medical, LLC
    Operator Number
    9043339
    Address
    2 Hampshire Street, Suite 202
    City
    Foxborough
    State
    MA
    Postal Code
    02035
    Country
    US
    Correspondent
    David - Rose

    Products

    Device Name Product Code
    Orthopedic Stereotaxic Instrument OLO

    Proprietary Names

    TELIGEN Procedure Kit Pro TELIGEN System Navigation Ready Instruments TELIGEN Procedure Kit

    Establishment Types

    Manufacture Medical Device for Another Party (Contract Manufacturer)