Vela Operations USA is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Vela Operations USA - FDA 510(k) Cleared Devices
Recent clearances: Great Basin Toxigenic C. difficile Direct Test (CDF2)
1
Total
1
Cleared
0
Denied
Vela Operations USA has 1 FDA 510(k) cleared medical devices. Based in Salt Lake City, US.
Last cleared in 2023. Active since 2023. Primary specialty: Microbiology.
Browse the FDA 510(k) cleared devices submitted by Vela Operations USA Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Vela Operations USA
1 devices