BEUDAMED
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    JACE MODEL W550 WRIST CPM DEVICE

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    Instrument Case

    FDA UDI
    KATENA PRODUCTS, INC.·00841668110980·STERILIZING CASE PLASTIC LARGE

    Guided Surgery

    FDA UDI
    BICON, LLC·00813110028075·2.0 x 8.0mm Guided Pilot Drill

    F.A.S.T. 1

    FDA Adverse Event
    Other ·PYNG MEDICAL CORP.·Product code FMI·May 30, 2006

    CURVED FINGER SPLINT

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    SATURN 8000

    FDA 510(k)
    FDA Class 2 ·Radiology

    FASTI INTRAOSSEOUS INFUSION SYSTEM

    FDA Adverse Event
    Other ·PYNG MEDICAL CORP.·Product code FMI·June 10, 2009

    FAST1 INTRAOSSEOUS INFUSION SYSTEM

    FDA Adverse Event
    Other ·PYNG MEDICAL CORP.·Product code FMI·June 10, 2009

    FAST1 INTRAOSSEOUS INFUSION SYSTEM

    FDA Adverse Event
    Other ·PYNG MEDICAL CORP.·Product code FMI·June 10, 2009

    FAST1 INTRAOSSEOUS INFUSION SYSTEM

    FDA Adverse Event
    Other ·PYNG MEDICAL CORP.·Product code FMI·June 10, 2009

    FAST1 INTRAOSSEOUS INFUSION SYSTEM

    FDA Adverse Event
    Other ·PYNG MEDICAL CORP.·Product code FMI·June 10, 2009

    FAST1 INTRAOSSEOUS INFUSION SYSTEM

    FDA Adverse Event
    Other ·PYNG MEDICAL CORP.·Product code FMI·June 10, 2009

    FAST1 INTRAOSSEOUS INFUSION SYSTEM

    FDA Adverse Event
    Other ·PYNG MEDICAL CORP.·Product code FMI·June 10, 2009

    LOCKING SCREW

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·January 17, 2013

    AUTOMATED PD SET W/CASSETTE4 PRONG

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·December 10, 2010

    SUBQ

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code LWS·July 8, 2014

    M2A-MAGNUM 42-50MM TPR INSRT-3

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·January 27, 2020

    M2A-MAGNUM MOD HD SZ 42MM 42MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·October 30, 2019

    TAPERLOC POR FMRL 9X137

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDI·October 30, 2019

    KIMBERLY CLARK MIC GASTRO-ENTERIC FEEDING TUBE, 22F. Gastro-Enteric Feeding Tube.

    FDA Recall
    Terminated ·Kimberly-Clark Corporation·Product code KNT·December 21, 2011