Bioinspire Technologies, Incorporated
Country not established
- Devices
- 1
What Bioinspire Technologies, Incorporated makes
Bioinspire Technologies, Incorporated manufactures the SinuBand, a nasal device designed for sinus drainage and pressure relief.
The SinuBand is classified as a Class I medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
SinuBand Ref K160101
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Bioinspire Technologies, Incorporated have in the registry?
The registry currently lists 1 device for Bioinspire Technologies, Incorporated. Devices recorded under merged duplicate company entries are counted once.
Which registries list Bioinspire Technologies, Incorporated's devices?
Among its 1 most recently registered device, Bioinspire Technologies, Incorporated has devices listed in FDA 510(k) (1 device).
What risk classes do Bioinspire Technologies, Incorporated's devices fall under?
Among its 1 most recently registered device, the classes recorded for Bioinspire Technologies, Incorporated's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Bioinspire Technologies, Incorporated in the registry?
The most recently registered devices listed for Bioinspire Technologies, Incorporated include SinuBand.