BEUDAMED
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    MODIFIED COPE SUTURE ANCHOR

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    UNKNOWN

    FDA Adverse Event
    Injury ·COOK INC·Product code KNT·April 17, 2020

    SILICONE ELASTOMER INFUSION CATHETER

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    SeaSpine Vu a•POD Prime NanoMetalene Intervertebral Body Fusion Device, SeaSpine Vu a•POD Prime Intervertebral Body Fusion Device

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ADULT DUAL HEATED EVAQUA BREATHING CIRCUIT

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code BZE·June 15, 2014

    TRIDENT HEMISPHERICAL CLUSTER HOLE SHELL

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS CORK·Product code MEH·October 12, 2010

    ENTERALITE INFINITY ENTERAL FEEDING PUMP

    FDA Adverse Event
    Malfunction ·MOOG MEDICAL DEVICES GROUP·Product code LZH·November 14, 2012