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    NEUROMOD DEVICES LIMITED

    FDA registration
    NEUROMOD DEVICES LIMITED·1 product·🇮🇪 Ireland

    Lenire

    FDA UDI
    NEUROMOD DEVICES LIMITED·05391540580141·Lenire Tinnitus Treatment Device

    Lenire

    FDA UDI
    NEUROMOD DEVICES LIMITED·05391540581018·Lenire Tonguetip

    Lenire

    FDA UDI
    NEUROMOD DEVICES LIMITED·05391540580158·Lenire Tonguetip

    Lenire

    FDA UDI
    NEUROMOD DEVICES LIMITED·05391540582015·Lenire Tinnitus Treatment Device

    LENIRE

    FDA Adverse Event
    Injury ·NEUROMOD DEVICES LIMITED·Product code QVN·August 14, 2024

    LENIRE

    FDA Adverse Event
    Death ·NEUROMOD DEVICES LIMITED·Product code QVN·April 9, 2024

    LENIRE

    FDA Adverse Event
    Injury ·NEUROMOD DEVICES LIMITED·Product code QVN·June 12, 2024

    LENIRE

    FDA Adverse Event
    Injury ·NEUROMOD DEVICES LIMITED·Product code QVN·March 22, 2024

    LENIRE

    FDA Adverse Event
    Injury ·NEUROMOD DEVICES LIMITED·Product code QVN·November 14, 2023

    LENIRE

    FDA Adverse Event
    Injury ·NEUROMOD DEVICES LIMITED·Product code QVN·November 22, 2023

    LENIRE

    FDA Adverse Event
    Injury ·NEUROMOD DEVICES LTD/NEUROMOD DEVICES LIMITED·Product code QVN·March 21, 2024

    NUEROMOD LENIRE

    FDA Adverse Event
    Malfunction ·NUEROMOD / NEUROMOD DEVICES LIMITED·Product code QVN·January 10, 2024