One adverse event report was listed on the US Food and Drug Administration (FDA) Manufacturer and User Device Facility Experience (MAUDE) database. One person suffered a corneal abrasion 5 days after ...

This briefing describes the regulated use of the technology for the indication specified, in the setting described, and with any other specific equipment referred to. It is the responsibility of ...

Medical device company TearScience has received 510(k) clearance on the latest version of its evaporative dry eye treatment. The Morrisville, North Carolina company’s novel dry eye treatment initially ...

TearScience will tap up to a whopping $70 million in new financing to ramp up commercial marketing efforts for its dry eye treatment device. HealthCare Royalty Partners is the sole backer of the new ...