Skip to content

Eli Ezer EDC-2600

by U.S. Ophthalmic, L.L.C.

Eli Ezer EDC-2600 is a Class I device made by U.S. Ophthalmic, L.L.C., listed in FDA GUDID since 18 Oct 2018 (UDI-DI 00851158007553), 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 Number00851158007553 UDI-DI Date18 Oct 2018ListedStatusListed 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  • Withdrawn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
Eli Ezer
Generic name
Vision testing/training chart
Model / reference
EDC-2600
Primary DI / UDI-DI
00851158007553
FDA product code
HOX
GMDN term
Vision testing/training chart
Device class
Class I
Regulation number
886.1150
GUDID distribution status
In Commercial Distribution

Related devices

Category: Vision testing/training chart

Similar devices in this category

Other devices filed under Vision testing/training chart.

Other devices from U.S. Ophthalmic, L.L.C.

See all devices from U.S. Ophthalmic, L.L.C. →

Properties

  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)