Spinex, Inc. is one of 26109 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
1
Total
1
Cleared
0
Denied
Spinex, Inc. has 1 FDA 510(k) cleared medical devices. Based in Fremont, US.
Latest FDA clearance: Apr 2026. Active since 2026. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Spinex, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Spinex, Inc.
1 devices