510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K051104Substantially Equivalent

Eye See Multipurpose, No-Rub Contact Lens Solution

Lapis Lazuli, NV, Grand Junction CO / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K051104 is the FDA 510(k) clearance record for EYE SEE MULTIPURPOSE, NO-RUB CONTACT LENS SOLUTION, a class II device, cleared for Lapis Lazuli, NV on under FDA product code LPN (Accessories, Soft Lens Products). FDA records list one 510(k) clearance for Lapis Lazuli, NV. As of , FDA records show no recalls naming K051104.

Clearance record

Decision date
Received
(394 days to decision)
Product code
LPN Accessories, Soft Lens Products
Regulation
21 CFR 886.5928
Device class
Class II
Review panel
Ophthalmic
Applicant
Lapis Lazuli, NV 623 Glacier Dr., Grand Junction CO
510(k) summary
Summary PDF
Third party review
No

Clearances, product code LPN

Trailing 12 months
1 clearance under product code LPN in the twelve months to October 2026, August 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code LPN, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20261
September 20260
October 20260