Progenix, LLC
Country not established
- Devices
- 1
What Progenix, LLC makes
Progenix, LLC manufactures the Progenix Select Stim, a Class II medical device designed for nerve stimulation applications, likely intended for targeted muscle or nerve activation in clinical or therapeutic settings.
The company’s portfolio is regulated under the FDA’s 510(k) pathway as Class II devices, indicating moderate risk and requiring pre-market clearance. The device is listed in the FDA’s 510(k) database, and the manufacturer is based in the United States.
Catalogue
Progenix Select Stim Ref K242460
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Progenix, LLC have in the registry?
The registry currently lists 1 device for Progenix, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Progenix, LLC's devices?
Among its 1 most recently registered device, Progenix, LLC has devices listed in FDA 510(k) (1 device).
What risk classes do Progenix, LLC's devices fall under?
Among its 1 most recently registered device, the classes recorded for Progenix, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Progenix, LLC in the registry?
The most recently registered devices listed for Progenix, LLC include Progenix Select Stim.