Essilor Of America, Inc.
United Statesfrom the FDA registration address FDA FEI 1000058437
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Essilor® Stellest® Ref DEN250016
Regimes: De Novo Registry: De Novo
Company details
- FDA FEI number
- 1000058437
- Address
- 13555 N Stemmons Fwy, DALLAS, TX, 75234
Frequently asked questions
How many devices does Essilor Of America, Inc. have in the registry?
The registry currently lists 1 device for Essilor Of America, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Essilor Of America, Inc.'s devices?
Among its 1 most recently registered device, Essilor Of America, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Essilor Of America, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Essilor Of America, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Essilor Of America, Inc. in the registry?
The most recently registered devices listed for Essilor Of America, Inc. include Essilor® Stellest®.