Medical Device Reprocessing | Products

The U.S. FDA sets stringent quality and safety standards for the reprocessing industry that assure devices are “substantially equivalent” to the original device. Stryker Sustainability Solutions has satisfied all FDA regulatory requirements to reprocess the following medical devices within these clinical areas:

EP & Cardiovascular, Non-Invasive, Open, Unused & Expired OR: General Surgery, and OR: Orthopedic/Arthroscopic.