BEUDAMED
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    LTDT PATIENT LIFTER

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    Archon

    FDA UDI
    Nuvasive, Inc.·00887517076410·Archon Screw, 4.0x10mm Fixed Self Drill

    ANTENSE ANTI-TENSION DEVICE

    FDA 510(k)
    FDA Class 2 ·Neurology

    XTRACETEZE SURGICAL SKIN STAPLE REMOVER 2001

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

    ACRYSOF IQ TORIC

    FDA Adverse Event
    Injury ·ALCON RESEARCH, LTD. / HUNTINGTON·Product code HQL·June 9, 2014

    RADIAL JAW 4 BIOPSY FORCEPS

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - COSTA RICA·Product code FCL·October 27, 2010

    SYNCHROMED II

    FDA Adverse Event
    Death ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·December 21, 2012

    Copeland HA Resurfacing Head, MB/HA EAS Head; Item Nos. 11-114641 11-114642 11-114643 11-114644 11-114644S 11-114645 11-114646 11-114647 11-114648 11-114661 11-114662 11-114663 11-114664 11-114664S 11-114665 11-114666 11-114667 11-114668 11-114632 11-114633 Product Usage: Partial Shoulder Replacement.

    FDA Enforcement
    Class II ·Terminated·Zimmer Biomet, Inc.·December 4, 2019