Dornier Medtech America Inc (Dmta) - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Dornier Medtech America Inc (Dmta) has 1 FDA 510(k) cleared medical devices. Based in Kennesaw, US.
Latest FDA clearance: Dec 2025. Active since 2025. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Dornier Medtech America Inc (Dmta) Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Dornier Medtech America Inc (Dmta)
1 devices