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Illuminix Claricon Max

by Illuminix Industries LLC

Illuminix Claricon Max is a Class II device made by Illuminix Industries LLC, listed in FDA GUDID since 23 Jan 2024 (UDI-DI 00860010833247), registry data as of 22 Oct 2026.

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

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00860010833247 UDI-DI Date23 Jan 2024ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Illuminix
Generic name
Ophthalmic examination slit lamp
Model / reference
CLARICON MAX
Primary DI / UDI-DI
00860010833247
FDA product code
PUE
GMDN term
Ophthalmic examination slit lamp
Device class
Class II
Regulation number
886.1850
GUDID distribution status
In Commercial Distribution

Related devices

Category: Ophthalmic examination slit lamp

Similar devices in this category

Other devices filed under Ophthalmic examination slit lamp.

Other devices from Illuminix Industries LLC

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Properties

  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Serial number
  • Manufacturing date
Other properties (10, all answered No)