BEUDAMED
    7 results · 52ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters FDA Adverse Event ×

    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