Medical Device Manufacturer · US , Scottsdale , AZ

Orthoscan, Inc. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2005

Total

Cleared

Denied

Orthoscan, Inc. has 5 FDA 510(k) cleared medical devices. Based in Scottsdale, US.

Last cleared in 2021. Active since 2005. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by Orthoscan, Inc. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Intertek Testing Services as regulatory consultant.

Orthoscan, Inc. is one of 16362 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Orthoscan, Inc.

5 devices

1-5 of 5

Data Source

Sourced from the FDA 510(k) public files . 176,325 total devices indexed.

Last updated: May 22, 2026