BEUDAMED
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    DUAL COLOR NITRILE EXAMINATION GLOVES, POWDER FREE, NON-STERILE, TESTED FOR USE WITH CHEMOTHERAPY DRUGS AND FENTANYL

    FDA 510(k)
    FDA Class 1 ·General Hospital

    Ophthalmic Spatula

    FDA UDI
    KATENA PRODUCTS, INC.·00841668103210·INTRALASE FLAP LIFTER DOUBLE ENDED

    Sklar®

    FDA UDI
    SKLAR CORPORATION·10649111356018·SKLARLITE ROCH-PEAN CVD 6.25"

    INTRALASE FLAP LIFTER DOUBLE ENDED

    FDA Adverse Event
    Injury ·CORZA OPTHALMOLOGY (KATENA PRODUCTS INC.)·Product code HND·January 24, 2024

    DESS Dental Implants

    FDA 510(k)
    FDA Class 2 ·Dental

    3.0T 8-CHANNEL CERVICAL-THORACIC-LUMBAR (CTL) ARRAY COIL

    FDA 510(k)
    FDA Class 2 ·Radiology

    AUTOFEED HUMIDIFICATION CHAMBER

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE, LTD.·Product code BTT·November 13, 2008

    DEXTRUS 4137

    FDA Adverse Event
    Injury ·BIOTRONIK SE & CO. KG·Product code NVZ·August 19, 2011

    NC QUANTUM APEX?

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code LOX·July 18, 2013