BEUDAMED
    10 results · 54ms · Sources: EU EUDAMED, US FDA

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    EZLASE SOFT TISSUE DENTAL LASER

    FDA Adverse Event
    Malfunction ·BIOLASE TECHNOLOGY, INC.·Product code GEX·December 28, 2007

    WATERLASE MD SOFT AND HARD TISSUE LASER

    FDA Adverse Event
    Other ·BIOLASE TECHNOLOGY, INC.·Product code GEX·December 9, 2008

    LASERWHITE 20 WHITENING GEL

    FDA Adverse Event
    Injury ·BIOLASE TECHNOLOGY, INC.·Product code GEX·February 8, 2011

    DIOLASE PLUS

    FDA Adverse Event
    Other ·BIOLASE TECHNOLOGY, INC.·Product code GEX·October 31, 2006

    DIOLASE PLUS

    FDA Adverse Event
    Injury ·BIOLASE TECHNOLOGY, INC.·Product code GEX·March 28, 2005

    LASERWHITE 20 WHITENING GEL

    FDA Adverse Event
    Malfunction ·BIOLASE TECHNOLOGY, INC.·Product code GEX·October 19, 2011

    LASERSMILE

    FDA Adverse Event
    Other ·BIOLASE TECHNOLOGY, INC.·Product code GEX·March 30, 2009

    Waterlase MD, dental laser unit, Model #6200218, serial numbers 10500210 to 105202680, inclusive.

    FDA Recall
    Terminated ·Biolase Technology Inc·Product code LYB·January 17, 2005

    WaterLase iPlus Dental Laser System, Part No. 7200854-XX Software Upgrade Kit, Part No. 6201463.

    FDA Recall
    Terminated ·Biolase Technology Inc·Product code GEX·June 12, 2014

    WaterLase iPlus Dental Laser System, Part No. 7200854-XX Software Upgrade Kit, Part No. 6201463.

    FDA Enforcement
    Class II ·Terminated·Biolase Technology Inc·August 27, 2014