Skip to content

Henry Schein 2020360

by Henry Schein, Inc.

Henry Schein 2020360 is a Class II device made by Henry Schein, Inc., listed in FDA GUDID since 24 Sep 2016 (UDI-DI 00304040016831), 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 Number00304040016831 UDI-DI Date24 Sep 2016ListedStatusListed 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  • Withdrawn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
Henry Schein
Generic name
Endodontic filling/sealing material
Model / Ref / Catalog
2020360
Description
CHANNELS MTA RC SEALER    EA
Primary DI / UDI-DI
00304040016831
FDA product code
KIF
GMDN term
Endodontic filling/sealing material
Device class
Class II
Regulation number
872.3820
GUDID distribution status
In Commercial Distribution
Size
Weight — 30 Gram

Related devices

Category: Endodontic filling/sealing material

Similar devices in this category

Other devices filed under Endodontic filling/sealing material.

Other devices from Henry Schein, Inc.

See all devices from Henry Schein, Inc. →

Properties

  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (10, all answered No)