Venclose digiRF Generator (VCRFG1)

Venclose digiRF Generator (VCRFG1) is an FDA 510(k)-cleared medical device (K250068) manufactured by Venclose, Inc.. 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 February 3, 2025. Regulation: 8.