Bright Uro, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Bright Uro, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Glean Urodynamics System Male Delivery System (GUS-1000-M), Glean Urodynamics System Male Delivery System (GUS-1000-M)
2
Total
2
Cleared
0
Denied
Bright Uro, Inc. has 2 FDA 510(k) cleared medical devices. Based in Irvine, US.
Latest FDA clearance: Apr 2026. Active since 2025. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Bright Uro, 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 - Bright Uro, Inc.
2 devices