BEUDAMED
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    Route 92 Medical Full Length 070 Access System

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    FASTIN PANACRYL

    FDA UDI
    DEPUY MITEK, LLC·10886705008292·FASTIN RC Anchor with PANACRYL Titanium Anchor ...

    THE JUDGE ROTENBERG EDUCATIONAL CENTER, INC.

    FDA registration
    THE JUDGE ROTENBERG EDUCATIONAL CENTER, INC.·1 product·🇺🇸 United States

    Med-Link Temp-pulse Oximeter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    REPROCESSED DISPOSABLE TROCARS

    FDA 510(k)
    FDA Class 1 ·Ear, Nose, Throat

    BD VACUTAINER® SODIUM HEPARIN (NH) BLOOD COLLECTION TUBES

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (BROKEN BOW)·Product code JKA·April 12, 2024

    TAXUS EXPRESS

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CARDIOVASCULAR DIVISION·Product code NIQ·October 30, 2008

    PROXIMATE** RELOADABLE LINEAR STAPLER - 30 MM

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·August 25, 2011

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·July 12, 2013

    SpF PLUS-Mini (60 ¿A/W) Implantable Spinal Fusion Stimulator SpF PLUS-Mini Implantable Fusion Stimulators are indicated as a spinal fusion adjunct to increase the probability of fusion success in 1 or 2 levels

    FDA Enforcement
    Class I ·Terminated·Zimmer Biomet, Inc.·November 7, 2018