PENTAX Medical’s Duodenoscope Receives FDA Clearance

DEC Duodenoscope has been approved by the FDA for use with the STERRAD 100NX Sterilizer from Advanced Sterilization Products (ASP), a division of Fortive, according to PENTAX Medical, a division of the HOYA Group. This development represents a significant advancement in infection prevention, as the DEC Duodenoscope is the first gastrointestinal endoscope compatible with hydrogen peroxide gas plasma sterilization, a cutting-edge technology in medical sterilization. The collaboration between PENTAX Medical and ASP aims to address the challenges of duodenoscope reprocessing, focusing on reducing the risk of cross-contamination and improving patient safety.

The FDA clearance of the DEC Duodenoscope marks PENTAX Medical's second major milestone in enhancing infection prevention. The first was the introduction of the disposable elevator cap, designed to reduce the risk of contamination while maintaining the high performance of reusable duodenoscopes. PENTAX Medical continues to lead in developing innovative solutions that align with the healthcare community's goals of improving patient outcomes, increasing efficiency, and reducing healthcare costs. Through its partnerships and focus on clinically relevant innovations, PENTAX Medical is committed to improving the quality of patient care and healthcare delivery.

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