Feg Textiltechnik Forschungs- Und Entwicklungsgesellschaft is one of 387 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Feg Textiltechnik Forschungs- Und Entwicklungsgesellschaft - FDA 510(...
Recent clearances: DynaMesh-POSTERIOR, DynaMesh-VENTRAL
2
Total
2
Cleared
0
Denied
Feg Textiltechnik Forschungs- Und Entwicklungsgesellschaft has 2 FDA 510(k) cleared medical devices. Based in Aachen, DE.
Historical record: 2 cleared submissions from 2016 to 2018. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Feg Textiltechnik Forschungs- Und Entwicklungsgesellschaft Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Meddiquest Limited and Meddiquest Regulatory Affairs, Ltd..
FDA 510(k) Regulatory Record - Feg Textiltechnik Forschungs- Und Entwicklungsgesellschaft
2 devices