BEUDAMED
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    AlphaID™ At Home Genetic Health Risk Service

    FDA 510(k)
    FDA Class 2 ·Immunology

    Foundation Surgical Interwedge

    FDA UDI
    FOUNDATION SURGICAL GROUP INC·00810141040366·Trial - 22x14x20

    Meridian

    FDA UDI
    Seaspine Orthopedics Corporation·10889981215521·No-Profile Interbody, 39mm x 27mm x 14mm, 20 Deg

    PARACON II/FECAL CONCENTRATOR II

    FDA 510(k)
    FDA Class 1 ·Microbiology

    Republic Spine Dark Star Spinal System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·November 3, 2014

    POWER PRO AMBULANCE COT

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code INK·August 16, 2011

    ACCU-CHEK ® SPIRIT COMBO

    FDA Adverse Event
    Malfunction ·ROCHE HEALTH SOLUTIONS, INC.·Product code LZG·July 11, 2013

    OT PING METER

    FDA Adverse Event
    Injury ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 20, 2013

    XP-XP Tibial Tray - Interlok 73 mm Item # 195756

    FDA Enforcement
    Class II ·Terminated·Zimmer Biomet, Inc.·September 18, 2019