Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

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

K-Number: K210930 · 2021-11-29

Decision Date2021-11-29
Product CodeLPL
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

ACUVUE® OASYS MAX 1-DAY Contact Lenses (senofilcon A) is a medical device manufactured by Johnson & Johnson Vision Care, Inc.. It received FDA 510(k) clearance on 2021-11-29 under approval number K210930. The device is classified under product code LPL. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

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.