Stryker Sustainability Solutions currently reprocesses/remanufactures devices in three key areas of the hospital: Cardiology/Electrophysiology, Operating Room, and Non-Invasive products. As preparation for FDA 510(k) pre-market notice submission, material characteristics, profiles and designs are evaluated and identified through reverse engineering and compared to predicate original devices. For mechanical design comparative research, bench and laboratory testing is conducted to demonstrate that reprocessed Stryker devices perform as originally intended. In addition, Stryker offers re-sterilization services for your Open, Unused and Expired products. To learn more about these clinical areas, please click on the boxes below.