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Ivotion Dent 742002

by Ivoclar Vivadent Aktiengesellschaft

Part of a family of 23 devices: see the family page

Ref 742002

Ivotion Dent 742002 is a device classified as Class IIa in the EU and Class II in the US made by Ivoclar Vivadent Aktiengesellschaft, registered in EUDAMED on 22 May 2026 (Basic UDI-DI 76152082APROS008W9) and listed in FDA GUDID since 4 Apr 2024 (UDI-DI 07615208314250), active as of 23 Oct 2026.

Active European Union. Also listed in GUDID (US).

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number76152082APROS008W9 Basic UDI-DI 07615208314250UDI-DIDate22 May 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number07615208314250 UDI-DI Date4 Apr 2024ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 76152082APROS008W9 registered 22 May 2026 Active
  • FDA GUDID UDI-DI 07615208314250 listed 4 Apr 2024 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 07615208314250
  2. Registered EUDAMED 76152082APROS008W9

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade name
Ivotion Dent Multi BL3 98.5-20mm/1 EUDAMED
Ivotion Dent GUDID
Generic name
Resin artificial teeth
Device name
Ivotion Dent, Ivotion Dent Multi
Model / Ref / Catalog
742002
Primary DI / UDI-DI
07615208314250
Basic UDI-DI
76152082APROS008W9
FDA product code
ELM
EMDN code
Q010699 Materials for the preparation of custom-made dental devices - other
GMDN term
Resin artificial teeth
Device class
Class IIa EUDAMED
Class II GUDID
Regulation number
872.3590
EU registration type
Standard device
EU market of registration
Liechtenstein
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class IIa
GUDID
Class II

Device class is stated on each registry's own scale: Class IIa in the EU (EUDAMED), Class II in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Related devices

Category: Resin artificial teeth

Similar devices in this category

Other devices filed under MATERIALS FOR THE PREPARATION OF CUSTOM-MADE DENTAL DEVICES - OTHER.

Other devices from Ivoclar Vivadent Aktiengesellschaft

See all devices from Ivoclar Vivadent Aktiengesellschaft →

Properties

  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (21, all answered No)