BEUDAMED
    87 results · 39ms · Sources: EU EUDAMED, US FDA

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    Sciton, Inc.

    Manufacturer
    🇺🇸 United States·1 Importer

    SCITON, INC.

    FDA registration
    SCITON, INC.·5 products·🇺🇸 United States

    BBLs

    FDA UDI
    SCITON, INC.·00863249000312·Intense pulsed light medical device

    JOULE

    FDA UDI
    SCITON, INC.·00863249000305·Multi-platform laser/light device for medical use.

    mJoule

    FDA UDI
    SCITON, INC.·00863249000329·Multi-platform laser/light device for medical use.

    RHYTEC PORTRAIT PSR3

    FDA Adverse Event
    Other ·RHYTEC, INC.·Product code GEI·October 14, 2006

    BBLS

    FDA Adverse Event
    Injury ·SCITON, INC.·Product code GEX·May 8, 2014

    PROFRACTIONAL HANDPIECE

    FDA Adverse Event
    Injury ·SCITON, INC.·Product code GEX·February 16, 2010

    PROFILE

    FDA Adverse Event
    Other ·SCITON, INC.·Product code GEX·February 16, 2010

    PROFILE

    FDA Adverse Event
    Other ·SCITON, INC.·Product code GEX·February 16, 2010

    PROFILE

    FDA Adverse Event
    Other ·SCITON, INC.·Product code GEX·February 16, 2010

    PROFILE

    FDA Adverse Event
    Other ·SCITON, INC.·Product code GEX·February 16, 2010

    PROFILE

    FDA Adverse Event
    Other ·SCITON, INC.·Product code GEX·February 16, 2010

    PROFILE

    FDA Adverse Event
    Other ·SCITON, INC.·Product code GEX·February 16, 2010

    PROFILE

    FDA Adverse Event
    Other ·SCITON, INC.·Product code GEX·February 16, 2010

    PROFILE

    FDA Adverse Event
    Other ·SCITON, INC.·Product code GEX·February 16, 2010

    PROFILE

    FDA Adverse Event
    Other ·SCITON, INC.·Product code GEX·February 16, 2010

    JOULE

    FDA Adverse Event
    Injury ·SCITON, INC.·Product code GEX·December 28, 2017

    DIVATYTE

    FDA Adverse Event
    Injury ·SCITON, INC.·Product code GEX·April 2, 2021

    MJOULE

    FDA Adverse Event
    Injury ·SCITON INC.·Product code GEX·September 10, 2024