Olleyes, Inc.
United Statesfrom the FDA registration address FDA FEI 3015867300
Olleyes, Inc. is a medical device manufacturer, with 2 devices listed in FDA GUDID (FDA Class I) as of 14 Nov 2026.
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
Registry facts
- Registries
- FDA GUDID 2
- Device classes
- FDA Class I 2
- Identifiers
- FDA FEI 3015867300
- DUNS 081297690
At a glance
Market reach
- United States
- FDA FEI
Catalogue
- Registry: GUDID
- Registry: GUDID
Company details
- FDA FEI number
- 3015867300
- DUNS number
- 081297690
- Address
- 350 Springfield Ave. Suite 200, Summit, NJ, 07901
- Website
- www.olleyes.com
- linkedin.com/company/olleyes-inc
- facebook.com/olleyes
- info@olleyes.com
- Phone
- 999-999-9999
From the company website
Olleyes Virtual Visual Field (includes Visual Acuity, Color, Contrast Sensitivity, Pupillometry, EOMS). Intuitive and easy to use products powered by AI.
Frequently asked questions
How many devices does Olleyes, Inc. have in the registry?
The registry currently lists 2 devices for Olleyes, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Olleyes, Inc.'s devices?
Among its 2 most recently registered devices, Olleyes, Inc. has devices listed in FDA GUDID (2 devices).
What risk classes do Olleyes, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Olleyes, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Olleyes, Inc. in the registry?
The most recently registered devices listed for Olleyes, Inc. include VisuALL VRP S 1 and VisuALL VRP ETS 1.