Ordinatrum Solutions is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ordinatrum Solutions - FDA 510(k) Cleared Devices
Recent clearances: ARC Intensive Care Information System (ARC System)
1
Total
1
Cleared
0
Denied
Ordinatrum Solutions has 1 FDA 510(k) cleared medical devices. Based in Tustin, US.
Last cleared in 2023. Active since 2023. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Ordinatrum Solutions Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Nilo Medical Consulting Group as regulatory consultant.
FDA 510(k) Regulatory Record - Ordinatrum Solutions
1 devices