Medical Device Manufacturer · US , Buffalo Grove , IL

Alma Lasers, Inc. - FDA 510(k) Cleared Devices

20 submissions · 20 cleared · Since 2010

Recent clearances: Alma TED+ System, Alma FemiLift Pixel CO2 Laser System, Delivery Devices and Accessories, The Alma Hybrid Laser System

20
Total
20
Cleared
0
Denied

Alma Lasers, Inc. has 20 FDA 510(k) cleared general & plastic surgery devices. Based in Buffalo Grove, US.

Latest FDA clearance: Jun 2026. Active since 2010.

Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.

Regulatory submissions have been managed by Kathy Maynor Consulting and Hogan Lovells US LLP.

FDA 510(k) Regulatory Record - Alma Lasers, Inc.

20 devices
1-12 of 20
Filters