BEUDAMED
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    VALLEYLAB FORCE FX

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

    MEDTRONIC MODEL 5301B TEST CABLE

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    SCENTED MENSTRUAL PAD

    FDA 510(k)
    FDA Class 1 ·Obstetrics/Gynecology

    SMALL CLIP APPLIER INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·February 5, 2013

    VITALITY 2

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·January 3, 2011

    CAPTIFLEX?

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - COSTA RICA (COYOL)·Product code FDI·July 18, 2014

    Philips Zenition 50, Model Number: 718096

    FDA Enforcement
    Class II ·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·November 20, 2024