Rhinix Aps
DenmarkFDA applicant, unverified
- Devices
- 1
What Rhinix Aps makes
Rhinix Aps manufactures nasal filters designed to reduce nasal congestion and improve breathing for patients with nasal airway obstruction or allergies. These single-use, disposable devices are intended for insertion into the nostrils to create a physical barrier that minimizes airflow resistance.
The nasal filter is classified as a Class II medical device under FDA regulations and is authorised via the 510(k) pathway. The company is based in the United States.
Catalogue
Rhinix Nasal Filter Ref K134003
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Rhinix Aps have in the registry?
The registry currently lists 1 device for Rhinix Aps. Devices recorded under merged duplicate company entries are counted once.
Which registries list Rhinix Aps's devices?
Among its 1 most recently registered device, Rhinix Aps has devices listed in FDA 510(k) (1 device).
What risk classes do Rhinix Aps's devices fall under?
Among its 1 most recently registered device, the classes recorded for Rhinix Aps's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Rhinix Aps in the registry?
The most recently registered devices listed for Rhinix Aps include RHINIX NASAL FILTER.