BEUDAMED
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    FDA 510(k)
    FDA Class 2 ·Neurology

    SUNPOLAR HEALTHLINE, MODEL 100; COMPFRESH, MODEL 200; NATUREX , MODEL 300; AND IHEALTH, MODEL 400 STOCKINGS

    FDA 510(k)
    FDA Class 2 ·General Hospital

    VASOPOUSE DEEP VEIN THROMBOSIS COMPRESSION DEVICE MODEL IPCS, MODEL SQS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CARELINK

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code KRG·October 10, 2014

    PRECISION®

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·July 15, 2011

    6000 CMS

    FDA Adverse Event
    Malfunction ·MOOG DEVICE GROUP·Product code FRN·May 13, 2013

    SENRI

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·April 2, 2021

    SENRI

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·July 9, 2019

    SENRI

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·July 11, 2024

    SENRI

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·February 20, 2020

    SENRI

    FDA Adverse Event
    Injury ·KANEKA·Product code LIT·March 12, 2019

    SENRI

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·May 6, 2025

    SENRI

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·December 24, 2025

    DIVA

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·July 7, 2020

    DIVA

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·July 7, 2020

    SHIRANUI EX

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·August 12, 2020

    18 SHIDEN HP

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·August 19, 2025

    SENRI

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·August 12, 2025

    18 SHIDEN HP

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·June 11, 2024

    SENRI EX

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·August 4, 2022