DEN250023 - Aurie System (FDA 510(k) Clearance)

DEN250023 is an FDA 510(k) submission (not cleared) for the Aurie System.

Submitted by Cathbuddy, Inc. (Syracuse, US). The FDA issued a Not Cleared (DENG) decision on April 30, 2026 after a review of 328 days.

This device falls under the Gastroenterology & Urology FDA review panel. The Traditional 510(k) pathway requires demonstration of substantial equivalence to a legally marketed predicate device - a standard the FDA determined was not met in this submission.

Device pattern: Regulatory edge-case submission. High predicate equivalence gap. With 328 days under review and no clearance granted, this submission reflects a case where the FDA could not confirm sufficient predicate equivalence - often indicating either a novel device category or unresolved safety and performance questions.

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