gi2000 Electrosurgical Generator

gi2000 Electrosurgical Generator is an FDA 510(k)-cleared medical device (K250657) manufactured by Cintron Medical 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 June 2, 2025. Regulation: 8.