BEUDAMED
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    RSM 1824C with RConsole1

    FDA 510(k)
    FDA Class 2 ·Radiology

    Oticon

    FDA UDI
    Oticon A/S·05707131305909·ACTO PRO, KIT 10 WL OMNI 85 BE RU

    TOTAL SHOULDER SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    VERTIFLEX SPINAL SCREW SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CERELINK ICP PROBE BASIC KIT

    FDA Adverse Event
    Injury ·INTEGRA LIFESCIENCES SWITZERLAND SAR·Product code GWM·January 23, 2023

    PAINSMART IOD

    FDA Adverse Event
    Malfunction ·MOOG DEVICE GROUP·Product code FRN·May 13, 2013

    ENDOTAK RELIANCE

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVY·July 14, 2011

    RESTORE ADVANCED RECHARGEABLE

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LGW·September 16, 2008