Vagatex
Country not established
- Devices
- 1
What Vagatex makes
Vagatex manufactures the VAGATEX device, a medical product designed for vaginal health applications, including tissue repair and support.
The VAGATEX device is classified as a Class II medical device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Vagatex Ref K782083
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Vagatex have in the registry?
The registry currently lists 1 device for Vagatex. Devices recorded under merged duplicate company entries are counted once.
Which registries list Vagatex's devices?
Among its 1 most recently registered device, Vagatex has devices listed in FDA 510(k) (1 device).
What risk classes do Vagatex's devices fall under?
Among its 1 most recently registered device, the classes recorded for Vagatex's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Vagatex in the registry?
The most recently registered devices listed for Vagatex include VAGATEX.