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Liquid Optics Interface Loi-12

by OptiMedica Corp.

Liquid Optics Interface Loi-12 is an ophthalmic laser system beam guide (FDA Class II; FDA product code OOE, Ophthalmic femtosecond laser) made by OptiMedica Corp., listed in FDA GUDID since 2 Sep 2016 (UDI-DI 05050474604810), 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 Number05050474604810 UDI-DI Date2 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  • Withdrawn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
Liquid Optics Interface
Generic name
Ophthalmic laser system beam guide
Model / Ref / Catalog
LOI-12
Primary DI / UDI-DI
05050474604810
FDA product code
OOE
GMDN term
Ophthalmic laser system beam guide
Device class
Class II
Regulation number
886.4390
GUDID distribution status
In Commercial Distribution

Related devices

Category: Ophthalmic laser system beam guide

Similar devices in this category

Other devices filed under Ophthalmic laser system beam guide.

Other devices from OptiMedica Corp.

See all devices from OptiMedica Corp. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)