BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Arklign Laboratories

    Reg #: 3006162709 · FEI: 3006162709 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    0
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    Arklign Laboratories
    Registration Number
    3006162709
    FEI Number
    3006162709
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    Yes
    Address
    2526 Qume Dr Ste 15
    City
    San Jose
    State
    CA
    ZIP
    95131
    Country
    US

    Regulatory Submissions

    510(k) Number
    K220835

    Owner / Operator

    Firm Name
    Arklign Laboratories
    Operator Number
    9098272
    Address
    2526 Qume Drive, Suite 15
    City
    San Jose
    State
    CA
    Postal Code
    95131
    Country
    US
    Correspondent
    Rex - Ho

    Products

    Device Name Product Code
    Aligner, Sequential NXC

    Establishment Types

    Manufacture Medical Device