Contact Lens Case— 510(k) K162869

Name: FDA 510(k) clearance K162869
Creator: U.S. Food and Drug Administration
Published: 2016-12-09

Substantially Equivalent

Ningbo Yinzhou Zonghai Artware Co., Ltd.

FDA 510(k) clearance K162869 for Contact Lens Case, Substantially Equivalent on 2016-12-09. Applicant: Ningbo Yinzhou Zonghai Artware Co., Ltd.. Device class: 2.

Clearance details

Applicant: Ningbo Yinzhou Zonghai Artware Co., Ltd.
Product code: Code LRX
Device class: Class 2
Regulation: 21 CFR 886.5928
Advisory panel: Ophthalmic
Date received: 2016-10-13
Decision date: 2016-12-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Ningbo City, CN

Download summary PDF View on FDA.gov ↗

Recent devices under product code LRX

view all

K252175 — LANDR Contact LENS Case2026-02-10
K250495 — MINI VP1 (PL67_F); MINI VP1 (PL61_F)2025-08-01
K240095 — CAREUS Contact Lens Case (Model 1, Model 2, Model 3, Model 4, Model 5, Model 6)2024-10-09
K231123 — Phoenix Contact Lens Case - dome top flat pack (CL-01) +2 more2023-08-30
K173538 — Clear Care Cleaning & Disinfecting Solution, AOCup Lens Case with AODisc2017-12-04

Data sourced from openFDA. This site is unofficial and independent of the FDA.