Tear Film Imager
Commercial- Indications
- Dry eye disease, COVID-19
Company intelligence / Profile preview
The company has commercialized the Tear Film Imager device for non-invasive measurement of tear film sublayers. The TFI has received FDA Class I exemption and initial commercialization efforts are focused on major academic medical centers in the U.S. Clinical results have been published in peer-reviewed journals; more than twenty patents granted globally.
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