Skip to content

FreshKon® (Methafilcon A) Alluring Eye, Mosaic, Colors Fusion

by Oculus Private Limited

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number08886428047382 UDI-DI Date15 Sep 2016ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
FreshKon® (Methafilcon A)
Generic Name
Soft corrective contact lens, daily-wear
Model / Reference
Alluring Eye, Mosaic, Colors Fusion
Primary DI / UDI-DI
08886428047382
FDA Product Code
LPL
GMDN Term
Soft corrective contact lens, daily-wear
Device Class
Class II
Regulation Number
886.5925
GUDID distribution status
In Commercial Distribution
Size
Outer Diameter — 14.2 Millimeter

Related devices

Category: Soft corrective contact lens, daily-wear

Other devices from Oculus Private Limited

Properties

  • Sterile
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (9)

  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No