New Cos Inc. Dba Visionair Solutions
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- Devices
- 1
What New Cos Inc. Dba Visionair Solutions makes
New Cos Inc. (dba Visionair Solutions) manufactures the VisionAir Patient-Specific Airway Stent, a customised airway stent designed to maintain patency in obstructed airways.
The device is classified as Class II under FDA regulations and is listed in the 510(k) clearance registry. The company is based in the United States.
Catalogue
VisionAir Patient-Specific Airway Stent Ref K213969
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does New Cos Inc. Dba Visionair Solutions have in the registry?
The registry currently lists 1 device for New Cos Inc. Dba Visionair Solutions. Devices recorded under merged duplicate company entries are counted once.
Which registries list New Cos Inc. Dba Visionair Solutions's devices?
Among its 1 most recently registered device, New Cos Inc. Dba Visionair Solutions has devices listed in FDA 510(k) (1 device).
What risk classes do New Cos Inc. Dba Visionair Solutions's devices fall under?
Among its 1 most recently registered device, the classes recorded for New Cos Inc. Dba Visionair Solutions's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from New Cos Inc. Dba Visionair Solutions in the registry?
The most recently registered devices listed for New Cos Inc. Dba Visionair Solutions include VisionAir Patient-Specific Airway Stent.