Prodeon Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Prodeon Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Urocross Expander System (Model Numbers ES2018 and ES3025), Prodeon Urethral Sheath System
3
Total
3
Cleared
0
Denied
Prodeon Medical, Inc. has 3 FDA 510(k) cleared medical devices. Based in Sunnyvale, US.
Latest FDA clearance: Jun 2026. Active since 2025. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Prodeon Medical, Inc. Filter by specialty or product code using the sidebar.
1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Prodeon Medical, Inc.
3 devices