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Henry Schein 9004802

by Henry Schein, Inc.

Henry Schein 9004802 is a dental amalgam well (FDA Class I; FDA product code EKI, Carrier, Amalgam, Operative) made by Henry Schein, Inc., listed in FDA GUDID since 5 Jul 2019 (UDI-DI 00304040067246), 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 Number00304040067246 UDI-DI Date5 Jul 2019ListedStatusListed 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  • Withdrawn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
Dental amalgam well
Model / Ref / Catalog
9004802
Primary DI / UDI-DI
00304040067246
FDA product code
EKI
GMDN term
Dental amalgam well
Device class
Class I
Regulation number
872.4565
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Dental amalgam well

Similar devices

Other devices filed under FDA product code EKI (CARRIER, AMALGAM, OPERATIVE).

Other devices from Henry Schein, Inc.

See all devices from Henry Schein, Inc. →

Properties

  • Supplied sterile
  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (10, all answered No)