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    HJY SMART MEDICAL DEVICE CO., LTD.

    FDA registration
    HJY SMART MEDICAL DEVICE CO., LTD.·3 products·🇹🇼 Taiwan

    HJY VisualNext Endoscopic Vision System

    FDA 510(k)
    FDA Class 2 ·Neurology

    HJY VisualNext 3D Endoscopic Vision System

    FDA 510(k)
    FDA Class 2 ·Neurology

    GRIESHABER DSP SURGICAL CONTACT LENS

    FDA Adverse Event
    Injury ·ALCON GRIESHABER AG·Product code HJI·June 12, 2023

    GRIESHABER DSP SURGICAL CONTACT LENS

    FDA Adverse Event
    Injury ·ALCON GRIESHABER AG·Product code HJI·June 13, 2023

    FUNDUS LASER LENS

    FDA Adverse Event
    Injury ·UNK·Product code HJI·November 17, 2021

    GRIESHABER DSP SURGICAL CONTACT LENS

    FDA Adverse Event
    Injury ·ALCON GRIESHABER AG·Product code HJI·June 13, 2023

    GRIESHABER DSP SURGICAL CONTACT LENS

    FDA Adverse Event
    Injury ·ALCON GRIESHABER AG·Product code HJI·June 23, 2023

    GRIESHABER DSP SURGICAL CONTACT LENS

    FDA Adverse Event
    Injury ·ALCON GRIESHABER AG·Product code HJI·June 26, 2023

    GRIESHABER DSP SURGICAL CONTACT LENS

    FDA Adverse Event
    Injury ·ALCON GRIESHABER AG·Product code HJI·June 29, 2023

    GRIESHABER DSP SURGICAL CONTACT LENS

    FDA Adverse Event
    Injury ·ALCON GRIESHABER AG·Product code HJI·June 13, 2023

    GRIESHABER DSP SURGICAL CONTACT LENS

    FDA Adverse Event
    Injury ·ALCON GRIESHABER AG·Product code HJI·June 13, 2023

    GRIESHABER DSP SURGICAL CONTACT LENS

    FDA Adverse Event
    Injury ·ALCON GRIESHABER AG·Product code HJI·June 13, 2023

    GRIESHABER DSP SURGICAL CONTACT LENS

    FDA Adverse Event
    Injury ·ALCON GRIESHABER AG·Product code HJI·June 13, 2023

    EBI XFIX DYNAFIX

    FDA Adverse Event
    Malfunction ·EBI MEDICAL SYSTEMS, INC.·Product code HJI·November 5, 1999

    GRIESHABER DSP SURGICAL CONTACT LENS

    FDA Adverse Event
    Injury ·ALCON GRIESHABER AG·Product code HJI·June 27, 2023

    Lombart 90D Clear with case Visualization during diagnosis and laser therapy of the human retina (fundus) using a slit lamp.

    FDA Recall
    Terminated ·Volk Optical Inc·Product code HJI·February 27, 2015

    Lens, Fundus, Hruby, Diagnostic

    FDA classification
    FDA Class 1 ·Lens, Fundus, Hruby, Diagnostic

    Reader, Bar, Ophthalmic

    FDA classification
    FDA Class 1 ·Reader, Bar, Ophthalmic

    H5i

    FDA UDI
    RESMED PTY LTD·00619498369010·H5i