Alma Lasers, Inc.
FDA 510(k) medical device clearances.
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.