BEUDAMED
    FDA Registration Active 🇯🇵 Japan

    Hand Held Auto Refract-Keratometer Retinomax K-plus5

    Reg #: 3004438257 · FEI: 3004438257 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    5
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    RIGHT MFG. CO., LTD.
    Registration Number
    3004438257
    FEI Number
    3004438257
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    1-47-3, Maenocho
    City
    Itabashi-Ku Tokyo
    Country
    JP

    Owner / Operator

    Firm Name
    RIGHT MFG. CO., LTD.
    Operator Number
    10036062
    Address
    1-47-3, Maenocho
    City
    Itabashi-ku
    State
    Tokyo
    Postal Code
    174-8633
    Country
    JP
    Correspondent
    Yasukatsu Oyama

    US Agent

    Business Name
    Visionix USA Inc.
    Contact Name
    Peter G. Sparacio
    Address
    160 Eisenhower Ln N
    City
    Lombard
    State
    IL
    ZIP
    60148
    Country
    US
    Email
    [email protected]
    Phone
    630 5090949

    Products

    Device Name Product Code
    Refractometer, Ophthalmic HKO

    Proprietary Names

    Hand Held Auto Refract-Keratometer Retinomax K-plus5 Hand Held Auto Refractometer Retinomax 5 Auto Refract-Keratometer Speedy-K2 Hand Held Auto Refractometer Retinomax Screeen Hand Held Auto Refract-Keratometer Retinomax K+Screeen

    Establishment Types

    Manufacture Medical Device