Blinktbi, Inc.
Country not established
- Devices
- 1
What Blinktbi, Inc. makes
Blinktbi, Inc. manufactures EyeStat, a medical device designed for ophthalmic diagnostic purposes, likely used to assess visual function or eye health metrics.
The company’s portfolio is regulated under FDA Class II devices, with EyeStat authorised via the 510(k) clearance pathway. The device is listed in the FDA’s 510(k) registry. Blinktbi, Inc. is based in the United States.
Catalogue
EyeStat Ref K191700
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Blinktbi, Inc. have in the registry?
The registry currently lists 1 device for Blinktbi, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Blinktbi, Inc.'s devices?
Among its 1 most recently registered device, Blinktbi, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Blinktbi, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Blinktbi, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Blinktbi, Inc. in the registry?
The most recently registered devices listed for Blinktbi, Inc. include EyeStat.