Erchonia Zerona® VZ8

Erchonia Zerona® VZ8 is an FDA 510(k)-cleared medical device (K243811) 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 January 9, 2025. Regulation: 8.