BEUDAMED
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    EDLENi Intra-Oral Sensor

    FDA 510(k)
    FDA Class 2 ·Dental

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517728067·CoRoent Large MP, 8x9x23mm 15°

    HHM

    FDA UDI
    Oticon A/S·05707131281654·H150V2, BTE 13 WL 100 SGR HHM

    DIRECT HDL CHOLESTEROL AND DIRECT HDL/LDL CALIBRATOR

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    WOUND PRO APEX

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    NC QUANTUM APEX?

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code LOX·August 20, 2025

    NC QUANTUM APEX?

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code LOX·February 5, 2026

    NC QUANTUM APEX

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code LOX·April 6, 2026

    NC QUANTUM APEX?

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code LOX·April 8, 2025

    NC QUANTUM APEX?

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code LOX·November 13, 2025

    NC QUANTUM APEX?

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code LOX·September 8, 2025

    NC QUANTUM APEX?

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code LOX·February 5, 2026

    NC QUANTUM APEX?

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code LOX·December 3, 2025

    NC QUANTUM APEX?

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code LOX·October 26, 2025

    NC QUANTUM APEX?

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code LOX·August 21, 2025

    NC QUANTUM APEX

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code LOX·March 25, 2025

    NC QUANTUM APEX

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code LOX·March 13, 2025

    PRISMAFLEX

    FDA Adverse Event
    Injury ·GAMBRO LUNDIA AB·Product code KDI·February 6, 2014

    PRISMAFLEX

    FDA Adverse Event
    Death ·GAMBRO LUNDIA AB·Product code KDI·April 11, 2014

    ASR UNI FEMORAL IMPL SIZE 49

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD. - 8010379·Product code KWA·June 6, 2013