Airess, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Airess, Inc. makes
Airess, Inc. manufactures non-prescription sunglasses and spectacle frames designed for general eyewear use.
These products are classified as Class I medical devices under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Non-Prescription Sunglasses Ref K935764
Regimes: 510(k) Registry: 510(k)Spectacle Frames Ref K934466
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Airess, Inc. have in the registry?
The registry currently lists 2 devices for Airess, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Airess, Inc.'s devices?
Among its 2 most recently registered devices, Airess, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Airess, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Airess, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Airess, Inc. in the registry?
The most recently registered devices listed for Airess, Inc. include NON-PRESCRIPTION SUNGLASSES and SPECTACLE FRAMES.