
Stryker Sustainability Solutions offers the industry’s most extensive and impactful medical device reprocessing and remanufacturing program through the integration of ultra-sonication and enzymatic cleaning with the technological advances of performance analysis to deliver clean, safe, functional and sterile OR devices.
In Stryker’s preparation for FDA 510(k) pre-market notice submission, material characteristics, profiles and designs are identified and evaluated through reverse engineering as well as compared to original devices. For mechanical design, comparative research, bench and laboratory testing is conducted to demonstrate that reprocessed Stryker devices perform as originally intended.