Codman Libertís Shunt Catheter with Bactiseal and Endexo Technology

Codman Libertís Shunt Catheter with Bactiseal and Endexo Technology is an FDA 510(k)-cleared medical device (K243531) manufactured by Integra Lifesciences Production Corporation. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 7, 2025. Regulation: 8.