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Ez 130700

by Centrix, Inc.

Ez 130700 is a Class I device made by Centrix, Inc., listed in FDA GUDID since 29 Dec 2023 (UDI-DI 00817051023724), 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 Number00817051023724 UDI-DI Date29 Dec 2023ListedStatusListed 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  • Withdrawn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
Ez
Generic name
Dental material cartridge-plunging applicator, single-component
Model / reference
130700
Primary DI / UDI-DI
00817051023724
FDA product code
EID
GMDN term
Dental material cartridge-plunging applicator, single-component
Device class
Class I
Regulation number
872.4565
GUDID distribution status
In Commercial Distribution

Related devices

Category: Dental material cartridge-plunging applicator, single-component

Similar devices

Other devices filed under FDA product code EID (Syringe, Restorative And Impression Material).

Other devices from Centrix, Inc.

See all devices from Centrix, Inc. →

Properties

  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (11, all answered No)