Promac
Country not established
- Devices
- 1
What Promac makes
Promac manufactures the FEMEX, a medical device designed for female pelvic health procedures, including mesh-related applications.
The FEMEX is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Femex Ref K812907
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Promac have in the registry?
The registry currently lists 1 device for Promac. Devices recorded under merged duplicate company entries are counted once.
Which registries list Promac's devices?
Among its 1 most recently registered device, Promac has devices listed in FDA 510(k) (1 device).
What risk classes do Promac's devices fall under?
Among its 1 most recently registered device, the classes recorded for Promac's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Promac in the registry?
The most recently registered devices listed for Promac include FEMEX.