Genossis, LLC
Country not established
- Devices
- 1
What Genossis, LLC makes
Genossis, LLC manufactures the OPTOSSOL Compression Device System, a medical device designed for compression therapy applications, typically used in the management of lymphedema or venous insufficiency.
The OPTOSSOL Compression Device System is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Optossol Compression Device System Ref K140875
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Genossis, LLC have in the registry?
The registry currently lists 1 device for Genossis, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Genossis, LLC's devices?
Among its 1 most recently registered device, Genossis, LLC has devices listed in FDA 510(k) (1 device).
What risk classes do Genossis, LLC's devices fall under?
Among its 1 most recently registered device, the classes recorded for Genossis, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Genossis, LLC in the registry?
The most recently registered devices listed for Genossis, LLC include OPTOSSOL COMPRESSION DEVICE SYSTEM.