Medical Device Manufacturer · US , Kennesaw , GA

Dornier Medtech America Inc (Dmta) - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2025
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)
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