Hinge Health, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Hinge Health, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Enso for Migraine, ENSO (Model 2)
2
Total
2
Cleared
0
Denied
Hinge Health, Inc. has 2 FDA 510(k) cleared medical devices. Based in San Francisco, US.
Latest FDA clearance: Apr 2026. Active since 2024. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Hinge Health, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Ebg Advisors, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Hinge Health, Inc.
2 devices