Ocusense, Inc.
Country not established
- Devices
- 1
What Ocusense, Inc. makes
Ocusense, Inc. manufactures the TearLab Osmolarity System, a diagnostic device designed to measure tear film osmolarity for assessing dry eye disease.
The device is classified as Class I under FDA regulations and is listed via a 510(k) clearance. Ocusense, Inc. is based in the United States.
Catalogue
Tearlab Osmolarity System Ref K083184
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ocusense, Inc. have in the registry?
The registry currently lists 1 device for Ocusense, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ocusense, Inc.'s devices?
Among its 1 most recently registered device, Ocusense, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Ocusense, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Ocusense, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Ocusense, Inc. in the registry?
The most recently registered devices listed for Ocusense, Inc. include TEARLAB OSMOLARITY SYSTEM.