Optomotor Laboratories
GermanyFDA applicant, unverified
- Devices
- 1
What Optomotor Laboratories makes
Optomotor Laboratories manufactures the EXPRESSEYE, a device designed for visual function assessment, likely used in clinical or research settings to evaluate eye movement and visual acuity.
The EXPRESSEYE is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Expresseye Ref K992473
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Optomotor Laboratories have in the registry?
The registry currently lists 1 device for Optomotor Laboratories. Devices recorded under merged duplicate company entries are counted once.
Which registries list Optomotor Laboratories's devices?
Among its 1 most recently registered device, Optomotor Laboratories has devices listed in FDA 510(k) (1 device).
What risk classes do Optomotor Laboratories's devices fall under?
Among its 1 most recently registered device, the classes recorded for Optomotor Laboratories's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Optomotor Laboratories in the registry?
The most recently registered devices listed for Optomotor Laboratories include EXPRESSEYE.