FDA 510(k) Applications Submitted by MARK ROHRER

FDA 510(k) Number Submission Date Device Name Applicant
K110304 02/02/2011 APEX ER. YAG / IPL SYSTEM SANDSTONE MEDICAL TECHNOLOGIES LLC
K110502 02/22/2011 TRIPLEX ER. YAG / ND: YAG SYSTEM SANDSTONE MEDICAL TECHNOLOGIES, LLC
K210535 02/24/2021 UltraLight LED System Rohrer Aesthetics, LLC
K180654 03/13/2018 PINXEL-RF system Rohrer Aesthetics, LLC
K110897 03/30/2011 CORTEX CO2 / ER:YAG LASER SYSTEM SANDSTONE MEDICAL TECHNOLOGIES, LLC
K100893 03/31/2010 CHEVEUX DIODE LASER SYSTEM SANDSTONE MEDICAL TECHNOLOGIES, LLC
K121162 04/17/2012 POLARIS Q-SWITCH RUBY SYSTEM SANDSTONE MEDICAL TECHNOLOGIES, LLC
K081219 04/30/2008 APOLLO MINI IPL SYSTEM SANDSTONE MEDICAL TECHNOLOGIES, LLC
K191162 05/01/2019 EpiLaze Multi-wavelength Laser Rohrer Aesthetics, LLC
K082101 07/25/2008 LS FAMILY OF CO2 LASERS WITH SCANNING HANDPIECE SANDSTONE MEDICAL TECHNOLOGIES, LLC
K212331 07/27/2021 BodySculp Rohrer Aesthetics, LLC
K082407 08/21/2008 MODIFICATION TO ULTRALIGHT II ND: YAG LASER SYSTEM SANDSTONE MEDICAL TECHNOLOGIES, LLC
K032599 08/25/2003 MEDICAL LASER TECHNOLOGIES, LLC MTL ERBIUM:YAG LASER SYSTEM MEDICAL LASER TECHNOLOGIES, LLC
K192583 09/19/2019 PicoLazer Laser System Rohrer Aesthetics, LLC
K093793 12/10/2009 LS-40 CO2 LASER SYSTEM MODEL LS-40 SANDSTONE MEDICAL TECHNOLOGIES, LLC
K123777 12/10/2012 MULTILASER SYSTEM ULTRALIGHT LASER TECHNOLOGIES, LLC


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