BEUDAMED
    FDA Registration Active 🇺🇸 United States

    EYEQUE CORPORATION

    Reg #: 3013003882 · FEI: 3013003882 · Expires 2026
    View on FDA
    Products
    8
    Proprietary Names
    16
    Establishment Types
    4
    Classifications
    8

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    Registration Details

    Registration Name
    EYEQUE CORPORATION
    Registration Number
    3013003882
    FEI Number
    3013003882
    Status
    Active
    Expiry Year
    2026
    Initial Importer
    No
    Address
    39608 Eureka Dr
    City
    Newark
    State
    CA
    ZIP
    94560
    Country
    US

    Owner / Operator

    Firm Name
    EYEQUE
    Operator Number
    10052589
    Address
    39608 Eureka Drive
    City
    Newark
    State
    CA
    Postal Code
    94560
    Country
    US
    Correspondent
    Noam Sapiens

    Products

    Device Name Product Code
    Refractor, Manual, Non-Powered, Including Phoropter HKN
    Frame, Trial, Ophthalmic HPA
    Chart, Visual Acuity HOX
    Medical Device Data System OUG
    Refractometer, Ophthalmic HKO
    Tester, Color Vision HIT
    Grid, Amsler HOQ
    Digital Visual Acuity Test QTO

    Proprietary Names

    PVT Lite EyeQue VERAI VERAI EyeQye PVT Lite EyeQue Try-On Glasses Try-On Glasses Insight Pro EyeQue Insight Lite Insight EyeQue Insight Insight Lite EyeQue Insight Pro EyeQue Connect EyeQue VisionCheck VisionCheck EyeQue Visual Acuity

    Establishment Types

    Remanufacture Medical Device Repack or Relabel Medical Device Develop Specifications But Do Not Manufacture At This Facility Manufacture Medical Device