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Durelon™ 38019

by 3M Deutschland GmbH 2 variants

Durelon™ 38019 is a Class II device made by 3M Deutschland GmbH, listed in FDA GUDID since 24 Sep 2016 (UDI-DI J001702011003130), 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 NumberJ001702011003130 UDI-DI Date24 Sep 2016ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Durelon™
Generic name
Zinc polycarboxylate dental cement
Model / Ref / Catalog
38019
Primary DI / UDI-DI
J001702011003130
FDA product code
EMA
GMDN term
Zinc polycarboxylate dental cement
Device class
Class II
Regulation number
872.3275
GUDID distribution status
In Commercial Distribution

Related devices

Category: Zinc polycarboxylate dental cement

Similar devices

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

Other devices from 3M Deutschland GmbH

See all devices from 3M Deutschland GmbH →

Properties

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