BEUDAMED
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    THE SHERLOCK 3CG TIP CONFIRMATION SYSTEM (TCS)

    FDA 510(k)
    FDA Class 2 ·General Hospital

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517637390·CoRoent Ant TLIF PEEK, 14x10x34mm 15°

    QCT Pro Asynchronous Calibration Module, CliniQCT

    FDA UDI
    MINDWAYS SOFTWARE, INC.·B052DIASYNC0·The QCT Pro Asynchronous Calibration Module is ...

    THOMS ALLIS TISSUE FORCEPS

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896023697·THOMS ALLIS TISSUE FORCEPS

    Hayden Medical

    FDA UDI
    Hayden Medical, Inc.·00840319740668·Vanderbilt University Vessel Clamp 8-1/2" (21.5cm)

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197053808·Overholt-Mixter Ligature Forceps curved...

    K140347

    FDA Adverse Event
    Injury ·DENTSPLY IMPLANTS (A DIVISION OF DENTSPLY IH AB)·Product code DZE·May 6, 2021

    K140347

    FDA Adverse Event
    Injury ·DENTSPLY IMPLANTS (A DIVISION OF DENTSPLY IH AB)·Product code DZE·May 6, 2021

    SYSTEMS INTEGRATION MODEL: ENDOALPHA

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    MODIFICATION TO NITREX NITINOL GUIDEWIRE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Truliant

    FDA UDI
    Exactech, Inc.·10885862315144·Truliant CR Porous Femoral

    GMK-SPHERE TIBIAL INSERT FIXED FLEX SIZE 2/10 MM RIGHT

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·August 18, 2017

    GMK SPHERE FEMORAL COMPONENT CEMENTED # 3 R

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL, SA·Product code JWH·July 31, 2015

    SECURE II MED/SURG BED

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FNL·May 31, 2013

    ZENITH RENU AAA ANCILLARY GRAFT MAIN BODY EXTENSION

    FDA Adverse Event
    Injury ·COOK, INC.·Product code MIH·June 16, 2011

    9617604-2008-00078

    FDA Adverse Event
    Malfunction ·Product code BTR·June 6, 2008

    GMK-SPHERE TIBIAL INSERT FIXED SPHERE FLEX SIZE 2/10 MM R

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·May 31, 2021

    SPECIFIC DEVICE NOT REPORTED

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·July 17, 2025

    TRULIANT

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·December 6, 2022

    HISTOACRYL FLEXIBLE PACK 5

    FDA Adverse Event
    Malfunction ·B. BRAUN SURGICAL SA·Product code MPN·February 11, 2020