BEUDAMED
    FDA Registration Active 🇺🇸 United States

    mild Device Kit

    Reg #: 3006450448 · FEI: 3006450448 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    1
    Establishment Types
    3
    Classifications
    1

    Registration Details

    Registration Name
    Vertos Medical Inc.
    Registration Number
    3006450448
    FEI Number
    3006450448
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    95 Enterprise Ste 325
    City
    Aliso Viejo
    State
    CA
    ZIP
    92656
    Country
    US

    Regulatory Submissions

    510(k) Number
    K093062

    Owner / Operator

    Firm Name
    STRYKER CORP.
    Operator Number
    1811755
    Address
    4100 East Milham Ave.
    City
    Kalamazoo
    State
    MI
    Postal Code
    49001
    Country
    US

    Products

    Device Name Product Code
    Arthroscope HRX

    Proprietary Names

    mild Device Kit

    Establishment Types

    Complaint File Establishment per 21 CFR 820.198 Develop Specifications But Do Not Manufacture At This Facility Manufacture Medical Device