BEUDAMED
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    Dymaxeon Spine System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    AGXO

    FDA UDI
    Oticon A/S·05707131285966·H150V2, RITE 312 WL TC AGXO

    Millennium

    FDA UDI
    Avalign Technologies, Inc.·00190776190682·Cuings Universal Retractor Small

    ESI

    FDA UDI
    FTT MEDICAL, INC.·B3961501840·HIRSCHMAN ANOSCOPE, LARGE 15/16" X 2-3/4". ACMI...

    Ophthalmic Speculum

    FDA UDI
    KATENA PRODUCTS, INC.·00841668100073·TEMPORAL SPECULUM SOLID BLADES

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197540414·Caspar Rongeur downwards angled 4x14mm 1 80mm

    ONE TOUCH ULTRA

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code CFR·November 21, 2003

    PULSAVAC®

    FDA UDI
    ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS, INC.·00889024374980·High Capacity Hip Revision Tip

    FUSTAR STEERABLE INTRODUCERS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    BIOGEL SKINSENSE POLY-ISOPRENE POWDER-FREE NON-LATEX GLOVE

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

    ENDOWRIST

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL, INC·Product code NAY·April 22, 2020

    ADVANTAGE SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·June 6, 2013

    ARCHITECT C8000 SYSTEM

    FDA Adverse Event
    Malfunction ·ABBOTT MANUFACTURING INC·Product code JJE·July 6, 2011

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·October 7, 2014

    6 Panel Cup Body and Lid w/Adult (AU), Item No. TDDA-6MBAU-CUP

    FDA Enforcement
    Class III ·Terminated·Ameditech Inc·December 30, 2015