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Ez3D-i v5.0

by Ewoosoft Co., Ltd.

Ez3D-i v5.0 is a Class II device made by Ewoosoft Co., Ltd., listed in FDA GUDID since 11 Jun 2018 (UDI-DI 08800019700098), 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 Number08800019700098 UDI-DI Date11 Jun 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  • Withdrawn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
Ez3D-i
Generic name
General-purpose dental x-ray system application software
Model / reference
v5.0
Primary DI / UDI-DI
08800019700098
FDA product code
LLZ
GMDN term
General-purpose dental x-ray system application software
Device class
Class II
Regulation number
892.2050
GUDID distribution status
In Commercial Distribution

Related devices

Category: General-purpose dental x-ray system application software

Similar devices in this category

Other devices filed under General-purpose dental x-ray system application software.

Other devices from Ewoosoft Co., Ltd.

  • EzOrtho

    Class IIa

  • Prora View

    Class IIa

  • Ez3D-i 5.5

    Class II

  • EzDent-i v2.1

    Class II

See all devices from Ewoosoft Co., Ltd. →

Properties

  • Prescription use
  • Lot / batch number
  • Manufacturing date
Other properties (12, all answered No)