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Sign in to claim this brandFeg Textiltechnik Forschungs- Und Entwicklungsgesellschaft
US
Last updated May 23, 2026
What Feg Textiltechnik Forschungs- Und Entwicklungsgesellschaft makes
Feg Textiltechnik develops synthetic mesh implants for hernia repair, including the DynaMesh-POSTERIOR and DynaMesh-VENTRAL, designed for posterior and ventral hernia reinforcement.
These products are classified as Class II devices under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What types of medical devices does Feg Textiltechnik develop?
Feg Textiltechnik specializes in the development of synthetic mesh implants intended for hernia repair. Their product portfolio includes specific solutions such as the DynaMesh-POSTERIOR and DynaMesh-VENTRAL, which are engineered to provide reinforcement for both posterior and ventral hernia conditions.
Where is Feg Textiltechnik based?
Feg Textiltechnik is based in the United States. This location serves as the primary base for the company's research and development activities regarding their synthetic mesh implant technologies.
How are the company's devices classified and regulated?
The devices developed by Feg Textiltechnik are classified as Class II medical devices under FDA regulations. These specific products are listed through the FDA 510(k) pathway, which is the regulatory process used to demonstrate that a device is substantially equivalent to a legally marketed predicate device.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
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Catalogue (4)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Dynamesh -cicat | K131530 | FDA 510(k) | Class II | Active |
| Dynamesh-Pp Standard, Model Pp02nnnn, Dynamesh-Pp Light, Model Pp01nnnn | K073579 | FDA 510(k) | Class II | Active |
| DynaMesh-POSTERIOR | K182087 | FDA 510(k) | Class II | Active |
| DynaMesh-VENTRAL | K161550 | FDA 510(k) | Class II | Active |
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