Alma Lasers, Inc.
Alma Lasers, Inc. holds FDA 510(k) medical device clearances, first cleared 2010, most recent 2026.
Top product codes for Alma Lasers, Inc.
Recent clearances by Alma Lasers, Inc.
- K251684 — Alma TED+ System
- K250071 — Alma FemiLift Pixel CO2 Laser System, Delivery Devices and Accessories
- K251230 — The Alma Hybrid Laser System
- K243044 — Alma Harmony
- K233024 — Alma Harmony
- K230308 — Alma Harmony
- K230371 — The Alma Soprano Titanium
- K222064 — The Alma Soprano Titanium
- K201520 — The Alma Opus System, Colibri Applicator and Tips
- K181298 — Harmony XL Multi-Application Platform
- K172193 — Modified Alma Lasers Soprano XL Family ofMulti-Application & Multi-Technology Platforms [SopranoXL, SopranoXLi, SopranoICE and Soprano ICE Platinum] with Duo and Trio Diode Laser Modules., Soprano Duo and Trio Diode Laser Modules
- K171242 — Alma LipoFlow System
- K170626 — Modified Alma Lasers Soprano XL Family of Multi-Application & Multi-Technology Platform, Soprano YAG Hand piece
- K160075 — Accent XL
- K121150 — ALMA LASERS FAMILY OF PIXEL RF TIPS
- K113810 — MODIFIED ALMA LASERS HARMONY 1064NM (ND:YAG) MODULES
- K112031 — ALMA LASERS MODIFIED DIODE LASER MODULE WITH SHR TREATMENT MODE FOR USE WITH THE FAMILY OF SOPRANO XL MULTI-APPLICATION
- K101147 — MODIFIED ALMA LASERS FAMILY OF ACCENT RADIOFREQUENCY (RF) SYSTEM
- K103501 — ALMA LASERS PIXEL CO2 LASER SYSTEM, DELIVERY DEVICE AND ACCESSORIES
- K102716 — MODIFIED ALMA LASERS FAMILY OF SOPRANO XL MULTI-APPLICATION PLATMFORMS
Data sourced from openFDA. This site is unofficial and independent of the FDA.