Medical Device Manufacturer · US , Omaha , NE

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

6 submissions · 6 cleared · Since 1994

Total

Cleared

Denied

Innovision, Inc. has 6 FDA 510(k) cleared medical devices. Based in Omaha, US.

Historical record: 6 cleared submissions from 1994 to 2015. Primary specialty: Orthopedic.

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

510(k) submissions have been managed by Musculoskeletal Clinical Regulatory Advisers, LLC as regulatory consultant.

Innovision, Inc. is one of 18477 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

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

6 devices

1-6 of 6

Data Source

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

Last updated: Sep 19, 2026