
ArthroCare Corporation
Free shipping on orders over $99 · 30-day returns
LYNX COBLATION Laryngeal Wand (72290254) is an FDA 510(k)-cleared medical device (K253680) manufactured by ArthroCare 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 March 24, 2026. Regulation: 8.