BEUDAMED
    FDA Registration Active 🇺🇸 United States

    VitreJect® LDS Safety Needle

    Reg #: 3012478173 · FEI: 3012478173 · Expires 2025
    View on FDA
    Products
    3
    Proprietary Names
    3
    Establishment Types
    1
    Classifications
    3

    Registration Details

    Registration Name
    OCUJECT, LLC
    Registration Number
    3012478173
    FEI Number
    3012478173
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    Yes
    Address
    13240 Evening Creek Dr S Ste 304
    City
    San Diego
    State
    CA
    ZIP
    92128
    Country
    US

    Regulatory Submissions

    510(k) Number
    K242956

    Owner / Operator

    Firm Name
    OcuJect, LLC
    Operator Number
    10051392
    Address
    1441 Avocado Avenue, Suite 204
    City
    Newport Beach
    State
    CA
    Postal Code
    92660
    Country
    US
    Correspondent
    Laurence Harvey

    Products

    Device Name Product Code
    Ophthalmic Needle QYM
    Needle, Hypodermic, Single Lumen FMI
    Low Dead Space Needle, Single Lumen, Hypodermic QNS

    Proprietary Names

    VitreJect® LDS Safety Needle OcuSafe® LDS Needle SteriCap® LDS Safety Needle

    Establishment Types

    Develop Specifications But Do Not Manufacture At This Facility