Rensihaw PLC
United KingdomFDA applicant, unverified
- Devices
- 1
What Rensihaw PLC makes
Rensihaw Plc manufactures the neuro inspire, a device designed for neuromodulation therapy to manage neurological conditions.
The neuro inspire is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
neuro inspire Ref K163666
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Rensihaw Plc have in the registry?
The registry currently lists 1 device for Rensihaw Plc. Devices recorded under merged duplicate company entries are counted once.
Which registries list Rensihaw Plc's devices?
Among its 1 most recently registered device, Rensihaw Plc has devices listed in FDA 510(k) (1 device).
What risk classes do Rensihaw Plc's devices fall under?
Among its 1 most recently registered device, the classes recorded for Rensihaw Plc's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Rensihaw Plc in the registry?
The most recently registered devices listed for Rensihaw Plc include neuro inspire.