510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K863129Substantially Equivalent

3M Corneal System (Corneal Preservation Medium)

3M Company, St. Paul MN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K863129 is the FDA 510(k) clearance record for 3M CORNEAL SYSTEM (CORNEAL PRESERVATION MEDIUM), cleared for 3M Company on under FDA product code LYX (Media, Corneal Storage). FDA records list 146 510(k) clearances for 3M Company, from to . As of , FDA records show no recalls naming K863129.

Clearance record

Decision date
Received
(33 days to decision)
Product code
LYX Media, Corneal Storage
Device class
Unclassified
Review panel
Unknown
Applicant
3M Company Bldg.S 251-3 And 270, St. Paul MN
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