
Vein 360, LLC
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Vein360 Endovenous Radiofrequency Ablation (RFA) Catheter is an FDA 510(k)-cleared medical device (K191073) manufactured by Vein 360, LLC. 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 October 21, 2019. Regulation: 8.