510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K131875Substantially Equivalent

Menicon Nect Contact Lens Case

Foresight Regulatory Strategies, Wilmington MA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K131875 is the FDA 510(k) clearance record for MENICON NECT CONTACT LENS CASE, a class II device, cleared for Foresight Regulatory Strategies on under FDA product code LRX (Case, Contact Lens). FDA records list one 510(k) clearance for Foresight Regulatory Strategies. As of , FDA records show no recalls naming K131875.

Clearance record

Decision date
Received
(43 days to decision)
Product code
LRX Case, Contact Lens
Regulation
21 CFR 886.5928
Device class
Class II
Review panel
Ophthalmic
Applicant
Foresight Regulatory Strategies 187 Ballardvale St., Suite 180, Wilmington MA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code LRX

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