
Venclose, Inc.
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Venclose digiRF Generator (VCRFG1); Venclose EVSRF Catheter (VC10A256F60, VC10A256F100) is an FDA 510(k)-cleared medical device (K252316) 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 August 18, 2025. Regulation: 8.