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Henry Schein 1001040

by Henry Schein, Inc.

Henry Schein 1001040 is a Class II device made by Henry Schein, Inc., listed in FDA GUDID since 24 Sep 2016 (UDI-DI 00304040004029), 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 Number00304040004029 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  • Withdrawn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
Zinc polycarboxylate dental cement
Model / Ref / Catalog
1001040
Primary DI / UDI-DI
00304040004029
FDA product code
EMA
GMDN term
Zinc polycarboxylate dental cement
Device class
Class II
Regulation number
872.3275
GUDID distribution status
In Commercial Distribution
Size
Weight — 40 Gram

Related devices

Category: Zinc polycarboxylate dental cement

Similar devices

Other devices filed under FDA product code EMA (CEMENT, DENTAL).

Other devices from Henry Schein, Inc.

See all devices from Henry Schein, Inc. →

Properties

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