Cognifisense, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cognifisense, Inc. has 2 FDA 510(k) cleared medical devices. Based in Sunnyvale, US.
Latest FDA clearance: Apr 2026. Active since 2023. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Cognifisense, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Cognifisense, Inc.
2 devices