Sinexus, Inc.
Country not established
- Devices
- 1
What Sinexus, Inc. makes
Sinexus, Inc. manufactures the Sinexus Sinus Stent Gen 2, a medical device designed for sinus drainage and ventilation, intended to improve airflow and reduce obstruction in nasal passages.
The company’s portfolio is regulated under Class I medical devices in the United States, with the Sinexus Sinus Stent Gen 2 listed via a 510(k) submission to the FDA. The company is based in the US.
Catalogue
Sinexus Sinus Stent Gen 2, Model 1999-25 Ref K092401
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Sinexus, Inc. have in the registry?
The registry currently lists 1 device for Sinexus, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sinexus, Inc.'s devices?
Among its 1 most recently registered device, Sinexus, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Sinexus, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Sinexus, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Sinexus, Inc. in the registry?
The most recently registered devices listed for Sinexus, Inc. include SINEXUS SINUS STENT GEN 2, MODEL 1999-25.