Dornier Medtech America Inc (Dmta) is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
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) Regulatory Record - Dornier Medtech America Inc (Dmta)
1 devices