510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K002319Substantially Equivalent

Purilens Saline Solution

Purilens, Inc., New Port Riche FL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K002319 is the FDA 510(k) clearance record for PURILENS SALINE SOLUTION, a class II device, cleared for Purilens, Inc. on under FDA product code LPN (Accessories, Soft Lens Products). FDA records list 2 510(k) clearances for Purilens, Inc., from to . As of , FDA records show no recalls naming K002319.

Clearance record

Decision date
Received
(30 days to decision)
Product code
LPN Accessories, Soft Lens Products
Regulation
21 CFR 886.5928
Device class
Class II
Review panel
Ophthalmic
Applicant
Purilens, Inc. 3234 Ella Ln., New Port Riche FL
510(k) summary
Summary
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