Onocor Vascular, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Onocor Vascular, LLC - FDA 510(k) Cleared Devices
Recent clearances: ONO Retrieval Device
1
Total
1
Cleared
0
Denied
Onocor Vascular, LLC has 1 FDA 510(k) cleared medical devices. Based in West Chester, US.
Last cleared in 2022. Active since 2022. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Onocor Vascular, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Onocor Vascular, LLC
1 devices