ACUVUE® OASYS MAX 1-DAY Contact Lenses (senofilcon A)
K-Number: K210930 · 2021-11-29
Device Summary
Frequently Asked Questions
What is the ACUVUE® OASYS MAX 1-DAY Contact Lenses (senofilcon A)?
ACUVUE® OASYS MAX 1-DAY Contact Lenses (senofilcon A) is a medical device that received FDA 510(k) clearance on 2021-11-29. It is manufactured by Johnson & Johnson Vision Care, Inc.. The 510(k) number is K210930.
When was ACUVUE® OASYS MAX 1-DAY Contact Lenses (senofilcon A) approved by the FDA?
ACUVUE® OASYS MAX 1-DAY Contact Lenses (senofilcon A) received FDA 510(k) clearance on 2021-11-29, under approval number K210930.
What company makes ACUVUE® OASYS MAX 1-DAY Contact Lenses (senofilcon A)?
ACUVUE® OASYS MAX 1-DAY Contact Lenses (senofilcon A) is manufactured by Johnson & Johnson Vision Care, Inc..
What is the FDA product code for ACUVUE® OASYS MAX 1-DAY Contact Lenses (senofilcon A)?
The FDA product code for ACUVUE® OASYS MAX 1-DAY Contact Lenses (senofilcon A) is LPL.
Related Clinical Trials
Other Devices by Johnson & Johnson Vision Care, Inc.
Related Devices (Code: LPL)
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.