Sapheneia Commercial Products AB
Country not established
- Devices
- 1
What Sapheneia Commercial Products AB makes
Sapheneia Commercial Products AB manufactures the SAPHENEIA CLARITY device, a Class II medical device.
The SAPHENEIA CLARITY device is regulated under the FDA 510(k) pathway and is listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
Sapheneia Clarity Ref K063391
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Sapheneia Commercial Products AB have in the registry?
The registry currently lists 1 device for Sapheneia Commercial Products AB. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sapheneia Commercial Products AB's devices?
Among its 1 most recently registered device, Sapheneia Commercial Products AB has devices listed in FDA 510(k) (1 device).
What risk classes do Sapheneia Commercial Products AB's devices fall under?
Among its 1 most recently registered device, the classes recorded for Sapheneia Commercial Products AB's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Sapheneia Commercial Products AB in the registry?
The most recently registered devices listed for Sapheneia Commercial Products AB include SAPHENEIA CLARITY.