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3M™ Espe™ 1919

by 3M Company

3M™ Espe™ 1919 is a Class I device made by 3M Company, listed in FDA GUDID since 24 Sep 2018 (UDI-DI 30605861032439), 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 Number30605861032439 UDI-DI Date24 Sep 2018ListedStatusListed 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  • Withdrawn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
3M™ Espe™
Generic name
Dental material application tool, single-use
Model / Ref / Catalog
1919
Primary DI / UDI-DI
30605861032439
FDA product code
KXR
GMDN term
Dental material application tool, single-use
Device class
Class I
Regulation number
872.3140
GUDID distribution status
In Commercial Distribution

Related devices

Category: Dental material application tool, single-use

Other devices from 3M Company

See all devices from 3M Company →

Properties

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