Urocure, LLC

Urocure, LLC — FDA 510(k) Submissions

Urocure, LLC has submitted 3 FDA 510(k) premarket notifications since 2019, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Mesh, Surgical, Synthetic, Urogynecologic, For Stress Urinary Incontinence, Retropubic Or Transobturator . Use the specialty filter in the sidebar to narrow results.