BEUDAMED
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    MAX-IF1000

    FDA 510(k)
    FDA Class 2 ·Neurology

    Alpen Carbides

    FDA UDI
    Dent4You AG·07630392905787·Alpen Carbides 246-FG-1.20-3.90, 10 pcs

    CEDIA Buprenorphine Controls

    FDA UDI
    Microgenics Corporation·00884883001756·

    METZENBAUM SCISSORS

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896046818·METZENBAUM SCISSORS CURVED BLADE

    Slip Free Zing String Elastometic Thread

    FDA UDI
    TP ORTHODONTICS INC·00192029039090·Heavy

    Hayden Medical

    FDA UDI
    Hayden Medical, Inc.·00840319736227·Potts-Smith Scissors 7-1/2" (18.8cm), angled on...

    Merit Medical®

    FDA UDI
    Merit Medical Systems, Inc.·00884450172117·

    Manta Ray™

    FDA UDI
    Seaspine Orthopedics Corporation·10889981056230·Plate - 2 Level - 46 mm

    Patella Trial

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215041793·

    CareLiving Pressure Activated Safety lancet 26G

    FDA UDI
    Care Living Diagnostics Inc.·00383568100246·Pressure Activated Safety lancet 26G*1.8mm,100p...

    RADIOCAMERAS EXTRACRANIAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    KYPHX INFLATABLE BONE TAMP, SIZE 20/3,MODEL K01A, KYPHX INFLATABLE BONE TAMP, SIZE 15/3, MODEL K02A

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    HEYER-SCHULTE BREAST IMPLANT

    FDA Adverse Event
    Injury ·V. MUELLER DIV. BAXTER HEALTHCARE CORP.·Product code FTR·June 10, 1994

    VERCISE GENUS?

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code MHY·August 25, 2025

    METRIX AIR

    FDA Adverse Event
    Malfunction ·TRIVIDIA HEALTH, INC.·Product code NBW·May 8, 2017

    OBTRYX SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·May 8, 2013

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·September 18, 2014

    INSTA TRAK 3500

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code IZL·May 16, 2011

    MEDTRONIC DUAL CHAMBER TEMPORARY EXTERNAL PACEMAKER 510(K) K150246

    FDA Adverse Event
    Death ·MEDTRONIC, INC.·Product code DTE·February 10, 2021

    VACUETTE TUBE9NC COAGULATION SODIUM CITRATE 3.2% 13X75

    FDA Adverse Event
    Malfunction ·GREINER BIO-ONE GMBH·Product code GIM·April 19, 2021