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EzCam-Cable

by Dentall co., Ltd.

EzCam-Cable is a Class I device made by Dentall co., Ltd., listed in FDA GUDID since 12 Aug 2020 (UDI-DI 08800096901326), registry data as of 12 Nov 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 12 Nov 2026.

Regulatory status

as of registry sync 12 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number08800096901326 UDI-DI Date12 Aug 2020ListedStatusListed 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  • Withdrawn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
EzCam
Generic name
Intraoral camera
Model / reference
EzCam-Cable
Primary DI / UDI-DI
08800096901326
FDA product code
KQM
GMDN term
Intraoral camera
Device class
Class I
Regulation number
878.4160
GUDID distribution status
In Commercial Distribution

Related devices

Category: Intraoral camera

Similar devices

Other devices filed under FDA product code KQM (Camera, Surgical And Accessories).

Other devices from Dentall co., Ltd.

See all devices from Dentall co., Ltd. →

Properties

  • Premarket exempt
Other properties (14, all answered No)