BEUDAMED
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    NASAL AIRWAY SPLINT

    FDA 510(k)
    FDA Class 1 ·Ear, Nose, Throat

    artegral

    FDA UDI
    Merz Dental GmbH·D7091972092·posteriors; shade C1; size L; upper jaw

    XPOD/XMAP NERVE STIMULATOR

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Reprocessed Shavers/Burs

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MENTOR SILTEX ROUND MODERATE PROFILE

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FWM·October 5, 2018

    AUTOPULSE NIMH BATTERY

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION, INC.·Product code DRM·January 22, 2013

    COULTER ACT DIFF ANALYZER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code GKZ·July 31, 2014

    ACCESS® 2 IMMUNOASSAY SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code JJE·January 27, 2011