Brain Sentinel, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Brain Sentinel, Inc. - FDA 510(k) Cleared Devices
Recent clearances: SPEAC System, SPEAC System
2
Total
2
Cleared
0
Denied
Brain Sentinel, Inc. has 2 FDA 510(k) cleared medical devices. Based in San Antonio, US.
Last cleared in 2021. Active since 2019. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Brain Sentinel, Inc. Filter by specialty or product code using the sidebar.
1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Brain Sentinel, Inc.
2 devices