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CediTEC DT 6088

by VOCO GmbH

Ref 6088Model disc

CediTEC DT 6088 is a device classified as Class IIa in the EU and Class II in the US made by VOCO GmbH, registered in EUDAMED on 17 Apr 2026 (Basic UDI-DI B-E22160881) and listed in FDA GUDID since 22 Oct 2021 (UDI-DI E22160881), active as of 22 Oct 2026.

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

CE MDD

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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-E22160881 Basic UDI-DI E22160881UDI-DIDate17 Apr 2026RegisteredStatusActive
United StatesGUDID listing GUDID NumberE22160881 UDI-DI Date22 Oct 2021ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-E22160881 registered 17 Apr 2026 Active
  • FDA GUDID UDI-DI E22160881 listed 22 Oct 2021 Listed

Timeline

2 dated events

  1. Listed FDA GUDID E22160881
  2. Registered EUDAMED B-E22160881

Coverage

2 jurisdictions

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  • Withdrawn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

Specification

EUDAMED · GUDID

Trade name
CediTEC DT
Generic name
Resin artificial teeth
Model / Ref / Catalog
6088, disc
Primary DI / UDI-DI
E22160881
Basic UDI-DI
B-E22160881
FDA product code
ELM
EMDN code
Q01020604 Orthodontic dental prostheses
GMDN term
Resin artificial teeth
Device class
Class IIa EUDAMED
Class II GUDID
Regulation number
872.3590
EU registration type
Legacy device (under a directive)
EU market of registration
Germany
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 DENTAL PROSTHESES (FOR DENTAL IMPLANTS SEE P010201).

Other devices from VOCO GmbH

See all devices from VOCO GmbH →

Properties

  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (18, all answered No)