FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Alma FemiLift Pixel CO2 Laser System, Delivery Devices and Accessories

K Number: K250071 · Decision Sep 24, 2025
Classifications
1
FEI Numbers
478
Registration Numbers
480
Same Product Code
2867
Applicant Total
20
Review Days
257

Basic Information

Device Name
Alma FemiLift Pixel CO2 Laser System, Delivery Devices and Accessories
K Number
K250071
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4810
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Alma Lasers, Inc.
Date Received
January 10, 2025
Decision Date
September 24, 2025
Product Code
GEX
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GEX Powered Laser Surgical Instrument

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (GEX), ordered by most recent decision date.

View all

Other Clearances by Alma Lasers, Inc.

K Number Device Name
K251684 Alma TED+ System
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
Search all 20 clearances from Alma Lasers, Inc. →