Dynapulse Medical - FDA 510(k) Cleared Devices

Dynapulse Medical has 1 FDA 510(k) cleared medical devices. Based in Minnetonka, US.

Latest FDA clearance: Dec 2025. Active since 2025. Primary specialty: Neurology.

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

510(k) submissions have been managed by MRC Global as regulatory consultant.