Oxus, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Oxus, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Oxus Sieve Beds
2
Total
2
Cleared
0
Denied
Oxus, Inc. has 2 FDA 510(k) cleared medical devices. Based in Auburn Hills, US.
Last cleared in 2023. Active since 2017. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Oxus, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Oxus, Inc. % Promedic, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Oxus, Inc.
2 devices