Brain Ultimate, Inc. is one of 16073 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Brain Ultimate, Inc. - FDA 510(k) Cleared Devices
Recent clearances: QuickVision Ultimate rTMS, Ultimate rTMS for OCD (M-series), Ultimate rTMS
4
Total
4
Cleared
0
Denied
Brain Ultimate, Inc. has 4 FDA 510(k) cleared medical devices. Based in Alpharetta, US.
Latest FDA clearance: Aug 2026. Active since 2023. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Brain Ultimate, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Makromed, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Brain Ultimate, Inc.
4 devices