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.

FDA 510(k) cleared devices by Renovo, Inc.

6 devices

1-6 of 6