FDA 510(k) Applications Submitted by ALMA LASERS, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K112031 07/15/2011 ALMA LASERS MODIFIED DIODE LASER MODULE WITH SHR TREATMENT MODE FOR USE WITH THE FAMILY OF SOPRANO XL MULTI-APPLICATION ALMA LASERS, INC.
K230308 02/03/2023 Alma Harmony Alma Lasers, Inc.
K101147 04/23/2010 MODIFIED ALMA LASERS FAMILY OF ACCENT RADIOFREQUENCY (RF) SYSTEM ALMA LASERS, INC.
K102716 09/21/2010 MODIFIED ALMA LASERS FAMILY OF SOPRANO XL MULTI-APPLICATION PLATMFORMS ALMA LASERS, INC.
K103501 11/29/2010 ALMA LASERS PIXEL CO2 LASER SYSTEM, DELIVERY DEVICE AND ACCESSORIES ALMA LASERS, INC.


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