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Quick Up 1626

by VOCO GmbH

Ref 1626

Quick Up 1626 is a device classified as Class IIa in the EU and Class II in the US made by VOCO GmbH, registered in EUDAMED on 30 Mar 2026 (Basic UDI-DI ++E2210363000000000DZ), cleared under FDA 510(k) K110440 on 4 May 2011 and listed in FDA GUDID since 31 Aug 2016 (UDI-DI E22116261), active as of 22 Oct 2026.

Active European Union and United States. Also listed in GUDID (US).

CE MDR 510(k)

Valid until

No date given

CE: no date in EUDAMED. FDA: not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

None linked in EUDAMED

A group certificate may exist

510(k) K110440

FDA submission, from GUDID

Trust

Unverified

Source EUDAMED, GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number++E2210363000000000DZ Basic UDI-DI E22116261UDI-DIDate30 Mar 2026RegisteredStatusActive
United StatesGUDID listing GUDID NumberE22116261 UDI-DI Date31 Aug 2016ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k) GUDID from GUDID NumberK110440 Date4 May 2011IssuedStatusActive

Official records

Across registries

3 registries list this device

  • EUDAMED Basic UDI-DI ++E2210363000000000DZ registered 30 Mar 2026 Active
  • FDA 510(k) K110440 decided 4 May 2011 Active
  • FDA GUDID UDI-DI E22116261 listed 31 Aug 2016 Listed

Timeline

3 dated events

  1. Cleared FDA 510(k) K110440
  2. Listed FDA GUDID E22116261
  3. Registered EUDAMED ++E2210363000000000DZ

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States FDA 510(k) Active

Specification

EUDAMED · GUDID

Trade name
Quick Up
Generic name
Denture reliner, hard
Model / Ref / Catalog
1626
Primary DI / UDI-DI
E22116261
Basic UDI-DI
++E2210363000000000DZ
510(k) Number
FDA product code
EBI
EMDN code
Q01020601 Mobile dental prostheses
GMDN term
Denture reliner, hard
Device class
Class IIa EUDAMED
Class II GUDID
Regulation number
872.3760
EU registration type
Standard device
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: Denture reliner, hard

Cleared under the same submission (K110440)

Similar devices

Also classified as Denture reliner, hard.

Similar devices in this category

Other devices filed under MOBILE DENTAL PROSTHESES.

Other devices from VOCO GmbH

See all devices from VOCO GmbH →

Properties

  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (22, all answered No)