Unicon Optical Co., Ltd.

FDA Regulatory Profile

Unicon Optical Co., Ltd. appears in FDA public data with 0 recalls, 5 510(k) clearances, 1 FDA inspection, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on July 12, 2024.

Summary

Total Recalls
0
510(k) Clearances
5
Inspections
1
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K241707OCuSOFT AMENITY™ (linofilcon A) DAILY DISPOSABLE CONTACT LENSES with HYDRASEAL™July 12, 2024
K213216Qualis (linofilcon A) Soft (Hydrophilic) Daily Wear Contact LensJanuary 18, 2022
K191929UNICON Hydrogel (Hioxifilcon A) Soft (Hydrophilic) Contact LensSeptember 17, 2019
K182734Unicon Hydrogel with Unicon Polymer (etafilcon A) Soft (Hydrophilic) Daily Disposable ContacMay 16, 2019
K141917UNICON (ETAFILCON A) SOFT (HYDROPHILIC) CONTACT LENS WITH UV BLOCKER FOR DAILY WEAROctober 17, 2014