BEUDAMED
    20 results · 51ms · Sources: EU EUDAMED, US FDA

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    SHARPLAN LASERS, INC. SILKTOUCH FLASH SCANNER

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

    SHARPLAN LASERS, INC. RUBY LASER SYSTEM

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

    SHARPLAN LASERS, INC. SURGICAL DIODE LASER

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

    SHARPLAN LASERS, INC. SILKTOUCH XJ SCANNER

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

    SHARPLAN LASERS, INC. SILKTOUCH CO2 FLASH SCANNER

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

    SHARPLAN LASERS, INC. AF ACUSPOT MICROMANIPULATOR (713)

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

    SHARPLAN LASERS, INC SILKTOUCH 2 FLASH SCANNER

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

    SHARPLAN LASERS, INC. PULSED CTH:YAG HOLMIUM SURGICAL LASER, MODEL 2040

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

    SHARPLAN

    FDA Adverse Event
    Death ·SHARPLAN LASERS, INC.·Product code GEX·February 8, 1994

    EPITOUCH ALEXANDRITE LASER

    FDA Adverse Event
    Other ·SHARPLAN LASERS INC.·Product code GEX·September 24, 2004

    SHARPLAN

    FDA Adverse Event
    Malfunction ·SHARPLAN LASERS INC.·Product code GEX·June 29, 1999

    SIDEFIRE

    FDA Adverse Event
    SHARPLAN LASERS, INC.·Product code GEX·April 28, 1995

    SHARPLAN

    FDA Adverse Event
    Injury ·SHARPLAN LASERS, INC.·Product code GEX·January 19, 2000

    SHARPLAN HEMISPHERICAL - 1000/160 MM STRAIGHT HAND PIECE

    FDA Adverse Event
    Injury ·SHARPLAN LASERS, INC.·Product code HRX·February 19, 1992

    SHARPLAN

    FDA Adverse Event
    Injury ·SHARPLAN LASERS, INC.·Product code GEX·September 14, 1994

    OTOLAM

    FDA Adverse Event
    Malfunction ·SHARPLAN LASERS, INC.·Product code EWG·November 24, 1999

    CARBON DIOXIDE LASER

    FDA Adverse Event
    Malfunction ·SHARPLAN LASERS, INC.·Product code GEX·May 13, 1994

    CO2 LASER, SHARPLAN

    FDA Adverse Event
    Malfunction ·SHARPLAN LASER, INC.·Product code HHR·July 26, 1996

    SHARPLAN

    FDA Adverse Event
    SHARPLAN LASER INC.·Product code LLO·July 29, 1994

    SHARPLASE DUAL EFFECT

    FDA Adverse Event
    Injury ·SHARPLIN LASERS, INC.·Product code HHR·August 9, 1995