Medical Device Manufacturer · US , Boston , MA

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

4 submissions · 4 cleared · Since 2018

Total

Cleared

Denied

Renovia, Inc. has 4 FDA 510(k) cleared medical devices. Based in Boston, US.

Last cleared in 2022. Active since 2018. Primary specialty: Gastroenterology & Urology.

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

4 devices

1–4 of 4

Data Source

FDA 510(k) public files . 174,402 total devices indexed.