Medical Device Manufacturer · US , Sunnyvale , CA

Prodeon Medical, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2025

Total

Cleared

Denied

Prodeon Medical, Inc. has 2 FDA 510(k) cleared medical devices. Based in Sunnyvale, US.

Latest FDA clearance: Mar 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.

2 devices

1-2 of 2