Product code LYX— Unknown
EUSOL-C
- Classification name
- Media, Corneal Storage
- Device class
- Unclassified
- Advisory panel
- Unknown
- Total cleared
- 21
- First cleared
- Most recent
Market context for product code LYX
FDA has cleared devices under product code LYX between 1982 and 2025, filed by 14 applicant companies. No FDA device recalls reference this product code.
Clearances per year
last 15 years- 2025
- 2022
- 2021
- 2016
- 2015
- 2007
- 2003
- 1996
- 1992
- 1990
- 1988
- 1987
- 1986
- 1985
- 1982
Top applicants under product code LYX
Recent clearances under product code LYX
- K251320 — XTRA4
- K221759 — Cornisol
- K211786 — Independent Corneal Viewing Chamber (IVC-21)
- K162013 — Eusol-C
- K151061 — Cornea Cold
- K063304 — LIFE4C
- K063617 — EUSOL-C
- K032422 — EUSOL-C
- K954548 — THE CHEN MEDIUM
- K924165 — OPTISOL-GS CORNEAL STORAGE MEDIA
- K921728 — DEXSOL CORNEAL STORAGE MEDIA CONTAINER, MODIFIED
- K921729 — OPTISOL CORNEAL STORAGE MEDIA CONTAINER/MODIFIED
- K894162 — OPTISOL
- K883854 — DEXSOL
- K870249 — MCCAREY-KAUFMAN CORNEAL STORAGE MEDIUM
- K870250 — MODIFIED MCCAREY-KAUFMAN CORNEAL STORAGE MEDIUM
- K870251 — CHONDROITIN SULFATE CORNEAL STORAGE MEDIUM
- K863129 — 3M CORNEAL SYSTEM (CORNEAL PRESERVATION MEDIUM)
- K854052 — CSM MEDIUM
- K844249 — K-SOL
- K821170 — CORNEA PERSERVATION UNIT
Data sourced from openFDA. This site is unofficial and independent of the FDA.