Optrascan, Inc. is one of 16310 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Optrascan, Inc. - FDA 510(k) Cleared Devices
Recent clearances: OptraSCAN System
1
Total
1
Cleared
0
Denied
Optrascan, Inc. has 1 FDA 510(k) cleared medical devices. Based in San Jose, US.
Latest FDA clearance: Jul 2026. Active since 2026. Primary specialty: Pathology.
Browse the FDA 510(k) cleared devices submitted by Optrascan, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Addwin Consulting as regulatory consultant.
FDA 510(k) Regulatory Record - Optrascan, Inc.
1 devices