Urocure, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Urocure, LLC - FDA 510(k) Cleared Devices
Recent clearances: ArcSP Suprapubic Sling System, ArcTO Transobturator Sling System, ArcTV Transvaginal Sling System
3
Total
3
Cleared
0
Denied
Urocure, LLC has 3 FDA 510(k) cleared medical devices. Based in Minneapolis, US.
Last cleared in 2022. Active since 2019. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Urocure, LLC Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Libramedical, Inc. and Libra Medial, Inc..
FDA 510(k) Regulatory Record - Urocure, LLC
3 devices