510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K033949Substantially Equivalent

Varilux Visionprint System (Vps)

Essilor Intl., Washington DC / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K033949 is the FDA 510(k) clearance record for VARILUX VISIONPRINT SYSTEM (VPS), a class II device, cleared for Essilor Intl. on under FDA product code HLL (Monitor, Eye Movement). FDA records list 2 510(k) clearances for Essilor Intl., from to . As of , FDA records show no recalls naming K033949.

Clearance record

Decision date
Received
(196 days to decision)
Product code
HLL Monitor, Eye Movement
Regulation
21 CFR 886.1510
Device class
Class II
Review panel
Ophthalmic
Applicant
Essilor Intl. 1301 K St., NW, Washington DC
510(k) summary
Summary PDF
Third party review
No

Clearances, product code HLL

Trailing 12 months

FDA records hold no clearances under product code HLL in the trailing twelve months.

FDA records show no clearances under product code HLL in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code HLL, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260