BEUDAMED
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    Uscan

    FDA 510(k)
    FDA Class 2 ·Radiology

    GMK-HINGE 02.09.0214H FIXED TIBIAL INSERT SIZE 2/14MM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code KRO·February 8, 2019

    ZOLL R SERIES

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ARK GABAPENTIN ASSAY, ARK GABEPENTIN CALIFRATOR, AND ARK GABAPENTIN CONTROL MODEL5025-0001-00, 5025-0002-00, 5025-0003-0

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    OPTI-FREE PLUS

    FDA Adverse Event
    Injury ·ALCON LABORATORIES, INC.·Product code LPN·December 12, 2017

    SUBDURAL ELECTRODES, DEPTH ELECTRODES, AND ANCHOR BOLTS

    FDA Adverse Event
    Injury ·AD-TECH MEDICAL INSTRUMENT CORP.·Product code GZL·June 14, 2019

    INFINITY DENTAL IMPLANT SYSTEM

    FDA Adverse Event
    Injury ·ACE SURGICAL SUPPLY CO.·Product code DZE·June 17, 2013

    HERCULES 3 STAGE WIREGUIDED BALLOON ESOPHAGEAL-PYLORIC-COLONIC

    FDA Adverse Event
    Malfunction ·WILSON-COOK MEDICAL INC·Product code KNQ·July 6, 2011

    ACCU-CHEK COMPACT TEST DRUM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·September 25, 2008