Savia Limited
Country not established
- Devices
- 1
What Savia Limited makes
Savia Limited manufactures the TENS Back Pain Relief System, a transcutaneous electrical nerve stimulation (TENS) device designed for managing chronic or acute back pain through low-voltage electrical impulses.
The TENS Back Pain Relief System is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Tens Back Pain Relief System Ref K113321
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Savia Limited have in the registry?
The registry currently lists 1 device for Savia Limited. Devices recorded under merged duplicate company entries are counted once.
Which registries list Savia Limited's devices?
Among its 1 most recently registered device, Savia Limited has devices listed in FDA 510(k) (1 device).
What risk classes do Savia Limited's devices fall under?
Among its 1 most recently registered device, the classes recorded for Savia Limited's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Savia Limited in the registry?
The most recently registered devices listed for Savia Limited include TENS BACK PAIN RELIEF SYSTEM.