510(k) K251230

Device
The Alma Hybrid Laser System
Applicant
Alma Lasers, Inc.
510(k) number
K251230
Product code
GEX
Decision
Substantially Equivalent (SESE)
Decision date
2025-05-21
Date received
2025-04-21
Regulation
878.4810
Classification name
Powered Laser Surgical Instrument
Medical specialty
General, Plastic Surgery
Review panel
General, Plastic Surgery
Device class
2
Clearance type
Special
Statement or summary
Summary
Third party reviewed
N

Related Records

Applicant Contact

Contact
Jessica Rivera-Montejo
Address
485 Half Day Rd. Suite 100 Buffalo Grove IL US 60089 60089

FDA Registration Numbers

Source Documents

510(k) summary PDF

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