Medical Device Manufacturer · US , Bend , OR

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

6 submissions · 6 cleared · Since 2017

Total

Cleared

Denied

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

Historical record: 6 cleared submissions from 2017 to 2018. Primary specialty: General & Plastic Surgery.

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

Regulatory submissions have been managed by Medical Device Academy, Inc. and Medical Devices Academy, Inc..

Renovo, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

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

6 devices

1-6 of 6

Data Source

Sourced from the FDA 510(k) public files . 175,218 total devices indexed.

Last updated: Jun 08, 2026