Rehasense USA, Inc. is one of 16362 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Rehasense USA, Inc. - FDA 510(k) Cleared Devices
Recent clearances: ICON 35
1
Total
1
Cleared
0
Denied
Rehasense USA, Inc. has 1 FDA 510(k) cleared medical devices. Based in Romeoville, US.
Latest FDA clearance: Jun 2026. Active since 2026. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Rehasense USA, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Shanghai SUNGO Management Consulting Co., Ltd. as regulatory consultant.
FDA 510(k) Regulatory Record - Rehasense USA, Inc.
1 devices