Tear Film Innovations, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K200400 | Systane iLux2 | May 21, 2020 |
| K172645 | iLux Instrument, iLux Disposable | December 26, 2017 |