BEUDAMED
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    Filters FDA Adverse Event × Regulation: Us FDA × Clear all

    MEDICAL DEVICE INTEGRATER SMARTLINX AXON 110

    FDA Adverse Event
    Malfunction ·CAPSULE TECH, INC.·Product code MHX·November 18, 2021

    YC-1800

    FDA Adverse Event
    Malfunction ·NIDEK CO., LTD.·Product code LXS·June 11, 2015

    TECNIS IOL

    FDA Adverse Event
    Malfunction ·AMO PUERTO RICO MFG. INC.·Product code MJP·December 5, 2023

    TECNIS IOL

    FDA Adverse Event
    Injury ·AMO PUERTO RICO MFG. INC.·Product code HQL·July 2, 2024

    TECNIS IOL

    FDA Adverse Event
    Malfunction ·AMO PUERTO RICO MFG. INC.·Product code MJP·November 22, 2024

    TECNIS IOL

    FDA Adverse Event
    Injury ·AMO MANUFACTURING NETHERLANDS·Product code HQL·February 6, 2021

    SENSAR IOL

    FDA Adverse Event
    Injury ·AMO PUERTO RICO MFG. INC.·Product code HQL·May 7, 2024