National Pain Institute
Country not established
- Devices
- 1
What National Pain Institute makes
The National Pain Institute manufactures the Pneumatherm, a medical device designed for thermal therapy applications in pain management, likely targeting procedures such as nerve ablation or tissue coagulation.
The Pneumatherm 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
Pneumatherm Ref K922089
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does National Pain Institute have in the registry?
The registry currently lists 1 device for National Pain Institute. Devices recorded under merged duplicate company entries are counted once.
Which registries list National Pain Institute's devices?
Among its 1 most recently registered device, National Pain Institute has devices listed in FDA 510(k) (1 device).
What risk classes do National Pain Institute's devices fall under?
Among its 1 most recently registered device, the classes recorded for National Pain Institute's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from National Pain Institute in the registry?
The most recently registered devices listed for National Pain Institute include PNEUMATHERM.