Koag, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Koag, LLC - FDA 510(k) Cleared Devices
Recent clearances: Vascette HP (hemostatic pad)
1
Total
1
Cleared
0
Denied
Koag, LLC has 1 FDA 510(k) cleared medical devices. Based in Vonore, US.
Last cleared in 2022. Active since 2022. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Koag, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Koag, LLC
1 devices