Kenneth Chapman
Country not established
- Devices
- 1
What Kenneth Chapman makes
Kenneth Chapman manufactures the MAXERECT, a device designed for erectile dysfunction treatment using vacuum therapy technology.
The MAXERECT is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Maxerect Ref K881008
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Kenneth Chapman have in the registry?
The registry currently lists 1 device for Kenneth Chapman. Devices recorded under merged duplicate company entries are counted once.
Which registries list Kenneth Chapman's devices?
Among its 1 most recently registered device, Kenneth Chapman has devices listed in FDA 510(k) (1 device).
What risk classes do Kenneth Chapman's devices fall under?
Among its 1 most recently registered device, the classes recorded for Kenneth Chapman's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Kenneth Chapman in the registry?
The most recently registered devices listed for Kenneth Chapman include MAXERECT.