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.

510(k) submissions have been managed by Bold Type as regulatory consultant. 1 device has linked clinical trial registered on ClinicalTrials.gov.

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

4 devices

1-4 of 4

Linked clinical trials FDA-regulated device evidence

Regulatory consultant 510(k) submission support ecosystem

Bold Type

Regulatory activity signals

510(k) clearance pathway relevance detected

Medical device regulatory intelligence node

Consulting ecosystem involvement present

Clinical validation data available

Data Source

Sourced from the FDA 510(k) public files . 174,883 total devices indexed.

Last updated: May 19, 2026