TauTona Pneumoperitoneum Assist Device (TPAD)

TauTona Pneumoperitoneum Assist Device (TPAD) is an FDA 510(k)-cleared medical device (K233020) manufactured by Tautona Group Research & Development, Co., LLC. This device is classified under the Obstetrics/Gynecology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 11, 2024. Regulation: 8.