BEUDAMED
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    TIPCAM 1S 3D System

    FDA 510(k)
    FDA Class 2 ·Neurology

    BRIGHTWAY TM BRAND NITRILE EXAMINATION GLOVES, POWDER FREE, NON-STERILE. (GREY COLOR)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    SUBDERMAL WIRE ELECTRODE, MODEL SWE

    FDA 510(k)
    FDA Class 2 ·Neurology

    BREATHTEK UBT KIT

    FDA Adverse Event
    Injury ·OTSUKA PHARMACEUTICAL DEVELOPMENT AND COMMERCIALIZ·Product code MSQ·October 8, 2014

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 15, 2011

    PAINSMART

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

    DEKA MOTUS AX

    FDA Adverse Event
    Injury ·EL.EN. ELECTRONIC ENGINEERING S.P.A.·Product code GEX·October 25, 2018

    DEKA MOTUS AX

    FDA Adverse Event
    Malfunction ·EL.EN. ELECTRONIC ENGINEERING S.P.A.·Product code GEX·March 9, 2023

    DEKA MOTUS AX

    FDA Adverse Event
    Malfunction ·EL.EN. ELECTRONIC ENGINEERING S.P.A.·Product code GEX·February 6, 2024

    XP-XP Tibial Tray - Interlok 63 mm Item # 195751

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