New Cos, Inc.
Country not established
- Devices
- 1
What New Cos, Inc. makes
New Cos, Inc. manufactures patient-specific airway stents designed to maintain or restore airway patency in clinical settings.
The company’s airway stents are classified as Class II devices under FDA regulations and are listed via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Patient-Specific Airway Stent Ref K182743
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does New Cos, Inc. have in the registry?
The registry currently lists 1 device for New Cos, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list New Cos, Inc.'s devices?
Among its 1 most recently registered device, New Cos, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do New Cos, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for New Cos, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from New Cos, Inc. in the registry?
The most recently registered devices listed for New Cos, Inc. include Patient-Specific Airway Stent.