TELLTALE Electrosurgical Guidewire System

TELLTALE Electrosurgical Guidewire System is an FDA 510(k)-cleared medical device (K252592) manufactured by Telltale, LLC. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 12, 2025. Regulation: 8.