BEUDAMED
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    Intense pulsed light therapy device

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

    Vu a-POD™

    FDA UDI
    Seaspine Orthopedics Corporation·10889981041762·27x21mm Trial Rasp 8mm 8 deg

    BIOMARC FIDUCIAL MARKER

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

    PLASTALGIN AND PLASTALGIN ORTHO

    FDA 510(k)
    FDA Class 2 ·Dental

    PINNACLE MTL INS NEUT40IDX56OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code KWA·August 18, 2011

    840 VENTILATOR

    FDA Adverse Event
    Malfunction ·PURITAN-BENNETT CORP·Product code CBK·November 14, 2008

    EASYTRAK 2

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code OJX·July 18, 2013

    Model Number L111, ESSENTIO DR SL MRI Pacemaker

    FDA Enforcement
    Class I ·Ongoing·Boston Scientific Corporation·October 22, 2025