Pro Axess
Country not established
- Devices
- 1
What Pro Axess makes
Pro Axess manufactures non-prescription sunglasses designed for general eye protection and UV radiation blocking. These products are intended for everyday use to reduce glare and shield the eyes from harmful sunlight.
The company’s portfolio is regulated under FDA’s Class I device category, requiring compliance with 510(k) clearance for market authorisation. The devices are listed in the FDA’s 510(k) database, adhering to U.S. regulatory standards for low-risk consumer eyewear.
Catalogue
Non-Prescription Sunglasses Ref K942588
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pro Axess have in the registry?
The registry currently lists 1 device for Pro Axess. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pro Axess's devices?
Among its 1 most recently registered device, Pro Axess has devices listed in FDA 510(k) (1 device).
What risk classes do Pro Axess's devices fall under?
Among its 1 most recently registered device, the classes recorded for Pro Axess's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Pro Axess in the registry?
The most recently registered devices listed for Pro Axess include NON-PRESCRIPTION SUNGLASSES.