Avenda Health, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Avenda Health, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Avenda Health AI Prostate Cancer Planning Software, Avenda Health Treatment System
2
Total
2
Cleared
0
Denied
Avenda Health, Inc. has 2 FDA 510(k) cleared medical devices. Based in Santa Monica, US.
Last cleared in 2022. Active since 2020. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Avenda Health, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Experien Group, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Avenda Health, Inc.
2 devices