Oculomotor Technologies
Country not established
- Devices
- 2
What Oculomotor Technologies makes
Oculomotor Technologies develops virtual-display software designed for routine eye exercise and rehabilitation, including products like OculoMotor Technologies and VERVE.
The company’s portfolio is regulated under FDA Class I devices, with products listed in the FDA’s 510(k) and UDI registries. The manufacturer is based in the United States.
Catalogue
- Registry: GUDID
Verve Ref K232930
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Oculomotor Technologies have in the registry?
The registry currently lists 2 devices for Oculomotor Technologies. Devices recorded under merged duplicate company entries are counted once.
Which registries list Oculomotor Technologies's devices?
Among its 2 most recently registered devices, Oculomotor Technologies has devices listed in FDA 510(k) (1 device) and FDA GUDID (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Oculomotor Technologies's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Oculomotor Technologies's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Oculomotor Technologies in the registry?
The most recently registered devices listed for Oculomotor Technologies include OculoMotor Technologies VERVE and VERVE.