BEUDAMED
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    SPECTRUM CURING LIGHT POLYMERIZATION UNIT

    FDA 510(k)
    FDA Class 2 ·Dental

    BASE

    FDA UDI
    Nuvasive, Inc.·00887517700742·BASE Ti HL Implant, 14x34x24mm 25°

    turbodent touch

    FDA 510(k)
    FDA Class 2 ·Dental

    NEXUS DETACHABLE COIL SYSTEM, HELIX SUPER SOFT CSR

    FDA 510(k)
    FDA Class 2 ·Neurology

    PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE

    FDA Adverse Event
    Malfunction ·MEDTRONIC MILACA, INC.·Product code LWP·February 9, 2013

    EASYTRAK 2

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code OJX·January 6, 2011

    PRECISION®

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·July 22, 2014