510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K844249Substantially Equivalent

K-Sol

Cilco, Inc., Huntington WV / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K844249 is the FDA 510(k) clearance record for K-SOL, cleared for Cilco, Inc. on under FDA product code LYX (Media, Corneal Storage). FDA records list 5 510(k) clearances for Cilco, Inc., from to . As of , FDA records show no recalls naming K844249.

Clearance record

Decision date
Received
(179 days to decision)
Product code
LYX Media, Corneal Storage
Device class
Unclassified
Review panel
Unknown
Applicant
Cilco, Inc. 1616 13th. Ave., Huntington WV
Third party review
No

Clearances, product code LYX

Trailing 12 months

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

FDA records show no clearances under product code LYX in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code LYX, 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