BEUDAMED
    FDA Registration Active 🇺🇸 United States

    NANOVIS INTERVERTEBRAL BODY FUSION SYSTEM

    Reg #: 1834379 · FEI: 1000306303 · Expires 2025
    View on FDA
    Products
    2
    Proprietary Names
    1
    Establishment Types
    1
    Classifications
    2

    Registration Details

    Registration Name
    MICROPULSE INC
    Registration Number
    1834379
    FEI Number
    1000306303
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    5865 E State Road 14
    City
    Columbia City
    State
    IN
    ZIP
    46725
    Country
    US

    Regulatory Submissions

    510(k) Number
    K110442

    Owner / Operator

    Firm Name
    Micropulse
    Operator Number
    10042100
    Address
    5865 E State Road 14
    City
    Columbia City
    State
    IN
    Postal Code
    46725
    Country
    US

    Products

    Device Name Product Code
    Intervertebral Fusion Device With Bone Graft, Cervical ODP
    Intervertebral Fusion Device With Bone Graft, Lumbar MAX

    Proprietary Names

    NANOVIS INTERVERTEBRAL BODY FUSION SYSTEM

    Establishment Types

    Manufacture Medical Device for Another Party (Contract Manufacturer)