Remi - FDA 510(k) Cleared Devices

Remi has 1 FDA 510(k) cleared medical devices. Based in San Francisco, US.

Latest FDA clearance: Oct 2025. Active since 2025. Primary specialty: Dental.

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

510(k) submissions have been managed by Prime Path Medtech as regulatory consultant.