Hnl Technologies
Country not established
- Devices
- 1
What Hnl Technologies makes
Hnl Technologies manufactures the MAXAIR Nasal Dilator System, a device designed to improve nasal airflow for patients with nasal obstruction or breathing difficulties.
The MAXAIR Nasal Dilator System is classified as a Class I medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Maxair Nasal Dilator System Ref K982929
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Hnl Technologies have in the registry?
The registry currently lists 1 device for Hnl Technologies. Devices recorded under merged duplicate company entries are counted once.
Which registries list Hnl Technologies's devices?
Among its 1 most recently registered device, Hnl Technologies has devices listed in FDA 510(k) (1 device).
What risk classes do Hnl Technologies's devices fall under?
Among its 1 most recently registered device, the classes recorded for Hnl Technologies's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Hnl Technologies in the registry?
The most recently registered devices listed for Hnl Technologies include MAXAIR NASAL DILATOR SYSTEM.