Erchonia CLX (Model # CFL)

Erchonia CLX (Model # CFL) is an FDA 510(k)-cleared medical device (K252574) manufactured by Erchonia Corporation. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 14, 2025. Regulation: 8.