ACUVUE® OASYS MAX 1-DAY Contact Lenses (senofilcon A)

ACUVUE® OASYS MAX 1-DAY Contact Lenses (senofilcon A) is an FDA 510(k)-cleared medical device (K210930) manufactured by Johnson & Johnson Vision Care, Inc.. This device is classified under the Ophthalmic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 28, 2021. Regulation: 8.