TrueTear Intranasal Tear Neurostimulator

TrueTear Intranasal Tear Neurostimulator is an FDA 510(k)-cleared medical device (K193589) manufactured by Allergan. This device is classified under the Ophthalmic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 30, 2020. Regulation: 8.