American Medtech
Country not established
- Devices
- 1
What American Medtech makes
American Medtech manufactures the REJOYN Penile Support System, a medical device designed to provide mechanical support for penile tissue. This device is intended for use in clinical settings to assist with conditions requiring structural support.
The REJOYN Penile Support System is classified as a Class II medical device and is listed in the FDA 510(k) registry. American Medtech is based in the United States.
Catalogue
Rejoyn Penile Support System Ref K971576
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does American Medtech have in the registry?
The registry currently lists 1 device for American Medtech. Devices recorded under merged duplicate company entries are counted once.
Which registries list American Medtech's devices?
Among its 1 most recently registered device, American Medtech has devices listed in FDA 510(k) (1 device).
What risk classes do American Medtech's devices fall under?
Among its 1 most recently registered device, the classes recorded for American Medtech's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from American Medtech in the registry?
The most recently registered devices listed for American Medtech include REJOYN PENILE SUPPORT SYSTEM.