Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Unicon Optical Co., Ltd. with 5 510(k) clearances. The most recent is a 510(k) clearance dated Jul 12, 2024: OCuSOFT AMENITY™ (linofilcon A) DAILY DISPOSABLE CONTACT LENSES with HYDRASEAL™.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Jul 12, 2024 | OCuSOFT AMENITY™ (linofilcon A) DAILY DISPOSABLE CONTACT LENSES with HYDRASEAL™K241707 · LPL | 510(k) clearances |
| Jan 18, 2022 | Qualis (linofilcon A) Soft (Hydrophilic) Daily Wear Contact LensK213216 · LPL | 510(k) clearances |
| Sep 17, 2019 | UNICON Hydrogel (Hioxifilcon A) Soft (Hydrophilic) Contact LensK191929 · LPL | 510(k) clearances |
| May 16, 2019 | Unicon Hydrogel with Unicon Polymer (etafilcon A) Soft (Hydrophilic) Daily Disposable ContacK182734 · LPL | 510(k) clearances |
| Oct 17, 2014 | UNICON (ETAFILCON A) SOFT (HYDROPHILIC) CONTACT LENS WITH UV BLOCKER FOR DAILY WEARK141917 · LPL | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
