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VisionX E7300

by Durr Dental AG 2 variants

VisionX E7300 (Version 4.0.x) is a Class II device made by Durr Dental AG, listed in FDA GUDID since 5 Dec 2019 (UDI-DI E247E7300), 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 NumberE247E7300 UDI-DI Date5 Dec 2019ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
VisionX
Generic name
General-purpose dental x-ray system application software
Model / Ref / Catalog
E7300, Version 4.0.x
Primary DI / UDI-DI
E247E7300
FDA product code
QIH
GMDN term
General-purpose dental x-ray system application software
Device class
Class II
Regulation number
892.2050
GUDID distribution status
In Commercial Distribution

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Properties

  • Prescription use
  • Lot / batch number
Other properties (13, all answered No)