Incisive, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Incisive, LLC - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Incisive, LLC has 2 FDA 510(k) cleared medical devices. Based in Richmond, US.
Historical record: 2 cleared submissions from 2001 to 2009. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Incisive, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Incisive, LLC
2 devices