Strauss Surgical Resection Instruments

Strauss Surgical Resection Instruments is an FDA 510(k)-cleared medical device (K253020) manufactured by American Medical Endoscopy, Inc.. 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 June 3, 2026. Regulation: 8.