Tear Film Innovations, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
iLux Instrument, iLux Disposable Ref K172645
Regimes: 510(k) Registry: 510(k)Systane iLux2 Ref K200400
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Tear Film Innovations, Inc. have in the registry?
The registry currently lists 2 devices for Tear Film Innovations, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Tear Film Innovations, Inc.'s devices?
Among its 2 most recently registered devices, Tear Film Innovations, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Tear Film Innovations, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Tear Film Innovations, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Tear Film Innovations, Inc. in the registry?
The most recently registered devices listed for Tear Film Innovations, Inc. include iLux Instrument, iLux Disposable and Systane iLux2.