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

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.