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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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