Dynapulse Medical is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Dynapulse Medical - FDA 510(k) Cleared Devices
Recent clearances: VEINOPLUS Back
1
Total
1
Cleared
0
Denied
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.
FDA 510(k) Regulatory Record - Dynapulse Medical
1 devices