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Resin Teeth DCL PE 608263

by Ivoclar Vivadent Aktiengesellschaft

Resin Teeth DCL PE 608263 is a Class II device made by Ivoclar Vivadent Aktiengesellschaft, listed in FDA GUDID since 28 Jan 2019 (UDI-DI DIVO6082631), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberDIVO6082631 UDI-DI Date28 Jan 2019ListedStatusListed 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  • Withdrawn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
Resin Teeth DCL PE
Generic name
Resin artificial teeth
Model / Ref / Catalog
608263
Primary DI / UDI-DI
DIVO6082631
FDA product code
ELM
GMDN term
Resin artificial teeth
Device class
Class II
Regulation number
872.3590
GUDID distribution status
In Commercial Distribution

Related devices

Category: Resin artificial teeth

Other devices from Ivoclar Vivadent Aktiengesellschaft

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Properties

  • Prescription use
  • Lot / batch number
Other properties (13, all answered No)