Uro-1, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Uro-1, Inc. - FDA 510(k) Cleared Devices
Recent clearances: SUREcore Plus Biopsy Instrument, VMCore Biopsy Needle, Repris Bladder Injection System
3
Total
3
Cleared
0
Denied
Uro-1, Inc. has 3 FDA 510(k) cleared medical devices. Based in Winston Salem, US.
Last cleared in 2022. Active since 2018. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Uro-1, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Uro-1, Inc.
3 devices