EYE SEE MULTIPURPOSE, NO-RUB CONTACT LENS SOLUTION— 510(k) K051104

Name: FDA 510(k) clearance K051104
Creator: U.S. Food and Drug Administration
Published: 2006-05-31

Substantially Equivalent

Lapis Lazuli, NV

FDA 510(k) clearance K051104 for EYE SEE MULTIPURPOSE, NO-RUB CONTACT LENS SOLUTION, Substantially Equivalent on 2006-05-31. Applicant: Lapis Lazuli, NV. Device class: 2.

Clearance details

Applicant: Lapis Lazuli, NV
Product code: Code LPN
Device class: Class 2
Regulation: 21 CFR 886.5928
Advisory panel: Ophthalmic
Date received: 2005-05-02
Decision date: 2006-05-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Grand Junction, CO, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code LPN

view all

K253795 — MeniSept 3% Hydrogen Peroxide Cleaning & Disinfecting Solution2026-08-13
K222541 — Bausch + Lomb Preservative Free Lubricating and Rewetting Drops2022-12-06
K221263 — Aqua Naina Plus Sterile Saline Solution2022-10-12
K202932 — ABT12 multi-purpose solution2021-05-28
K210051 — OTE MPS 045 Multi-purpose Lens Care Solution2021-05-26

Adverse events under product code LPN

product code LPN

Injury: 333
Other: 8
Total: 341

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

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