510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K070767Substantially Equivalent

Eye See Multipurpose Contact Lens Solution

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

K070767 is the FDA 510(k) clearance record for EYE SEE MULTIPURPOSE CONTACT LENS SOLUTION, a class II device, cleared for Lapis Lazuli International NV on under FDA product code LPN (Accessories, Soft Lens Products). FDA records list one 510(k) clearance for Lapis Lazuli International NV. As of , FDA records show no recalls naming K070767.

Clearance record

Decision date
Received
(126 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 International NV 2214 Sanford Dr. Suite B7, 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