Iasis Technologies is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Iasis Technologies - FDA 510(k) Cleared Devices
Recent clearances: IASIS i2 Relaxation Neurofeedback System
1
Total
1
Cleared
0
Denied
Iasis Technologies has 1 FDA 510(k) cleared medical devices. Based in Murrieta, US.
Latest FDA clearance: Mar 2026. Active since 2026. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Iasis Technologies Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Mdi Consultants, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Iasis Technologies
1 devices