E&E Optics, Inc.
Country not established
- Devices
- 1
What E&E Optics, Inc. makes
E&E Optics, Inc. manufactures rigid gas permeable contact lenses designed for daily wear, including models intended for orthokeratology (Ortho-K) to reshape the cornea overnight. These lenses are intended for extended wear applications, providing clear vision while allowing oxygen to pass through the material.
The company’s products are classified as Class II medical devices under FDA regulations and are authorised through the 510(k) pathway. These devices are listed in the FDA’s 510(k) database, reflecting their compliance with applicable US regulatory standards.
Catalogue
- 510(k) 510(k)
Frequently asked questions
How many devices does E&E Optics, Inc. have in the registry?
The registry currently lists 1 device for E&E Optics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list E&E Optics, Inc.'s devices?
Among its 1 most recently registered device, E&E Optics, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do E&E Optics, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for E&E Optics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from E&E Optics, Inc. in the registry?
The most recently registered devices listed for E&E Optics, Inc. include eLens Rigid Gas Permeable Contact Lens for Daily Wear, eLens Rigid Gas Permeable Contact Lens for Daily Wear Ortho-K.