Phoenix Contact Lens Case - dome top flat pack (CL-01) +2 more— 510(k) K231123

Name: FDA 510(k) clearance K231123
Creator: U.S. Food and Drug Administration
Published: 2023-08-30

Substantially Equivalent

Phoenix Innovative Healthcare Manufacturers Pvt. , Ltd.

FDA 510(k) clearance K231123 for Phoenix Contact Lens Case - dome top flat pack (CL-01) +2 more, Substantially Equivalent on 2023-08-30. Applicant: Phoenix Innovative Healthcare Manufacturers Pvt. , Ltd.. Device class: 2.

Clearance details

Device name as filed: Phoenix Contact Lens Case - dome top flat pack (CL-01); Phoenix Contact Lens Case - classic flat pack (CL-02); Phoenix Contact Lens Case - sunglass shape flat pack (CL-03)
Applicant: Phoenix Innovative Healthcare Manufacturers Pvt. , Ltd.
Product code: Code LRX
Device class: Class 2
Regulation: 21 CFR 886.5928
Advisory panel: Ophthalmic
Date received: 2023-04-20
Decision date: 2023-08-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Navi Mumbai, IN

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
K173538 — Clear Care Cleaning & Disinfecting Solution, AOCup Lens Case with AODisc2017-12-04
K172925 — Contact Lens Case, Model: A-1, B-12017-11-30

More clearances from Phoenix Innovative Healthcare Manufacturers Pvt. , Ltd.

view all

K201032 — Phoenix Digital Thermometer2021-10-29

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