510(k) K210930 · LPL Lenses, Soft Contact, Daily Wear
ACUVUE® OASYS MAX 1-DAY Contact Lenses (senofilcon A)
| Applicant | Johnson & Johnson Vision Care, Inc., Jacksonville FL, US |
| Decision | Substantially Equivalent, Nov 29, 2021 |
| Received | Mar 29, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K210930
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jul 23, 2025 | Johnson & Johnson Vision Care, Inc. ACUVUE OASYS MAX 1-Day MULTIFOCAL Open, Classified |
LPL | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.