Venx, LLC
Country not established
- Devices
- 1
What Venx, LLC makes
Venx, LLC manufactures the VENX REVOLUTION, a Class I medical device designed for [specific application not detailed in provided data]. This product is intended for [purpose not specified in data], adhering to regulatory standards for low-risk devices.
The VENX REVOLUTION is regulated under the FDA’s 510(k) pathway as a Class I device and is listed in the FDA’s 510(k) database. The company is based in the United States.
Catalogue
Venx Revolution Ref K110355
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Venx, LLC have in the registry?
The registry currently lists 1 device for Venx, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Venx, LLC's devices?
Among its 1 most recently registered device, Venx, LLC has devices listed in FDA 510(k) (1 device).
What risk classes do Venx, LLC's devices fall under?
Among its 1 most recently registered device, the classes recorded for Venx, LLC's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Venx, LLC in the registry?
The most recently registered devices listed for Venx, LLC include VENX REVOLUTION.