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# FDA Clears New Version of UroViu Endoscope
- URL: https://www.fdaweb.com/fda-clears-new-version-of-uroviu-endoscope/
- Published: 2025-09-30T12:00:00.000Z
- Updated: 2026-09-14T15:23:04.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5159964

FDA has cleared a UroViu 510(k) for its UV5000 cordless, single-use endoscope platform. The new device, which replaces the UV4500 currently on the market, is designed to improve clinical efficiency with a faster processor, longer battery life, and brighter high-definition visualization, according to the company.

UroViu says the UV5000 is compatible with the company’s range of single-use cannulas, graspers, and biopsy forceps, and is intended to streamline endoscopic procedures without the need for reusable scopes or reprocessing. UroViu has also filed a 510(k) that is seeking clearance for a Wi-Fi–enabled version, the UV5000W, which would allow direct streaming to external displays.