510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K222484Substantially Equivalent

Retitrack

C. Light Technologies, Inc., Medford MA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K222484 is the FDA 510(k) clearance record for Retitrack, a class II device, cleared for C. Light Technologies, Inc. on under FDA product code HLL (Monitor, Eye Movement). FDA records list one 510(k) clearance for C. Light Technologies, Inc. As of , FDA records show no recalls naming K222484.

Clearance record

Decision date
Received
(265 days to decision)
Product code
HLL Monitor, Eye Movement
Regulation
21 CFR 886.1510
Device class
Class II
Review panel
Ophthalmic
Applicant
C. Light Technologies, Inc. 84 High St., Suite 303, Medford MA
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