UroViu Receives FDA 510(k) Clearance for Its UV5000W Wi-Fi Enabled Advanced Endoscope Platform

UroViu Receives FDA 510(k) Clearance for Its UV5000W Wi-Fi Enabled Advanced Endoscope Platform

UroViu Corporation is pleased to announce that the U.S. Food and Drug Administration (FDA) has granted 510(k) clearance for its UV5000W Wi-Fi-enabled cordless, single-use endoscope platform.

The UV5000W combines the recently cleared UV5000 with a Wi-Fi relay, allowing connection to any external display. As Bruce OuYang, Ph.D., CEO of UroViu, commented, “The UV5000W setup now allows the clinician the option to keep his/her eyesight in the axis of operations, while the simultaneous external display allows visualization by the patients and other clinicians as needed. Clearance of the UV5000W Wi-Fi platform is a major advance in endoscopy that allows secure wireless connectivity within a busy and crowded procedure room.”

UroViu is committed to its goal to “Simplify the Scope of Patient Care” and revolutionizing embedded single-use visualization.

The UV5000W is immediately available in the U.S. market. For more information or to schedule a hands-on demonstration, please contact your UroViu’s sales representative or customer service as listed on our website: https://www.uroviu.com)