Medical Device Manufacturer · US , Fremont , CA

Devoro Medical, Inc. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2020

Total

Cleared

Denied

Devoro Medical, Inc. has 5 FDA 510(k) cleared medical devices. Based in Fremont, US.

Latest FDA clearance: May 2024. Active since 2020. Primary specialty: Cardiovascular.

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

510(k) submissions have been managed by Northwest Clinical Research Group, Inc. as regulatory consultant.

Devoro Medical, 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 - Devoro Medical, Inc.

5 devices

1-5 of 5

Data Source

Sourced from the FDA 510(k) public files . 175,450 total devices indexed.

Last updated: May 10, 2026