Freedom Laser Therapy, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Freedom Laser Therapy, Inc. - FDA 510(k) Cleared Devices
Recent clearances: ID-510 iRestore Elite, ID-500 iRestore Hair Growth System, iRestore Professional 282
4
Total
4
Cleared
0
Denied
Freedom Laser Therapy, Inc. has 4 FDA 510(k) cleared medical devices. Based in Los Angeles, US.
Last cleared in 2022. Active since 2016. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Freedom Laser Therapy, Inc. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Emergo Global Consulting, LLC and Nst Consultants, Inc..
FDA 510(k) Regulatory Record - Freedom Laser Therapy, Inc.
4 devices