Syncthink, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 2
What Syncthink, Inc. makes
Syncthink, Inc. makes EYE-SYNC, a device used for assessing eye movement and vestibular function, particularly in the context of concussion and neurological evaluation.
The EYE-SYNC device is classified as Class II and is listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Frequently asked questions
How many devices does Syncthink, Inc. have in the registry?
The registry currently lists 2 devices for Syncthink, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Syncthink, Inc.'s devices?
Among its 2 most recently registered devices, Syncthink, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Syncthink, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Syncthink, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Syncthink, Inc. in the registry?
The most recently registered devices listed for Syncthink, Inc. include EYE-SYNC.