BEUDAMED
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    OXYGEN MASK REBREATHER

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517361202·CoRoent SI Trial, 8x17x14mm

    discovery®

    FDA UDI
    DENTAURUM GmbH & Co.KG·J011790164000·discovery® Bracket, + 12° Torque, + 5° Angulati...

    CERALAS MULTIWAVELENGTH 980/1470NM DIODE LASER

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    CleverLock Guidewire Locking Device and Biopsy Cap

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

    SENSOR ENLITE

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code OZO·May 5, 2014

    CARELINK PROGRAM W/TELEMETRY C

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code DXY·October 15, 2012

    FREESTYLE

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC, USA·Product code NBW·August 17, 2007

    PROPONENT DR SL (Model L201)

    FDA Enforcement
    Class I ·Ongoing·Boston Scientific Corporation·October 22, 2025