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ARCUSevo 1.005.0900

by KaVo Dental GmbH

Part of a family of 6 devices: see the family page

Ref 1.005.0900

ARCUSevo 1.005.0900 is a Class I device made by KaVo Dental GmbH, registered in EUDAMED on 26 Jun 2026 (Basic UDI-DI ++EKAVG440Z8) and listed in FDA GUDID since 26 Sep 2016 (UDI-DI EKAV100509000), active as of 24 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 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number++EKAVG440Z8 Basic UDI-DI EKAV100509000UDI-DIDate26 Jun 2026RegisteredStatusActive
United StatesGUDID listing GUDID NumberEKAV100509000 UDI-DI Date26 Sep 2016ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI ++EKAVG440Z8 registered 26 Jun 2026 Active
  • FDA GUDID UDI-DI EKAV100509000 listed 26 Sep 2016 Listed

Timeline

2 dated events

  1. Listed FDA GUDID EKAV100509000
  2. Registered EUDAMED ++EKAVG440Z8

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  • Withdrawn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
ARCUSevo
Generic name
Facebow
Device name
articulator, facebow
Model / Ref / Catalog
1.005.0900
Primary DI / UDI-DI
EKAV100509000
Basic UDI-DI
++EKAVG440Z8
FDA product code
EJP
EMDN code
Q010401 Orthodontic face bows
GMDN term
Facebow
Device class
Class I
Regulation number
872.3150
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution

Related devices

Category: Facebow

Similar devices in this category

Other devices filed under ORTHODONTIC FACE BOWS.

Other devices from KaVo Dental GmbH

See all devices from KaVo Dental GmbH →

Properties

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