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Flents 68090

by Apothecary Products, Inc.

Flents 68090 is a contact lens case (FDA Class II; FDA product code LRX, Case, Contact Lens) made by Apothecary Products, Inc., listed in FDA GUDID since 6 Sep 2016 (UDI-DI 00025715680903), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00025715680903 UDI-DI Date6 Sep 2016ListedStatusListed 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  • Withdrawn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
Flents
Generic name
Contact lens case
Model / reference
68090
Primary DI / UDI-DI
00025715680903
FDA product code
LRX
GMDN term
Contact lens case
Device class
Class II
Regulation number
886.5928
GUDID distribution status
In Commercial Distribution

Related devices

Category: Contact lens case

Similar devices

Other devices filed under FDA product code LRX (Case, Contact Lens).

Other devices from Apothecary Products, Inc.

See all devices from Apothecary Products, Inc. →

Properties

  • Single use
  • Over-the-counter
  • Lot / batch number
Other properties (12, all answered No)