BEUDAMED
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    WILLIAMS VERTEBRAL SPREADER

    FDA 510(k)
    FDA Class 1 ·Orthopedic

    TC-PLUS PRIMARY KNEE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PreOp

    FDA 510(k)
    FDA Class 2 ·Neurology

    M2A-MAGNUM PF CUP 46ODX40ID

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·June 13, 2014

    LIGAMAX-5MM

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code FZP·October 18, 2010

    ULTRACISION HARMONIC ACE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·December 13, 2012

    Biograph 16, Biograph PET/CT Scanner, Catalog No. 872858, Manufactured by Siemens Medical Solutions USA, Inc., 810 Innovation Drive, Knoxville, TN 37932 USA, TEL: 865-218-2534

    FDA Recall
    Terminated ·Siemens Medical Solutions USA Inc·Product code KPS·July 23, 2007