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Abutments Try-in

by JJGC Indústria e Comércio de Materiais Dentários S.A 77 variants

Part of a family of 77 devices: see the family page

Ref 114.784Model Abutment

Abutments Try-in (114.784) is a Class I device made by JJGC Indústria e Comércio de Materiais Dentários S/A., registered in EUDAMED on 6 May 2026 (Basic UDI-DI 987800049VV) and listed in FDA GUDID since 13 Dec 2022 (UDI-DI 07899878029267), active as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number987800049VV Basic UDI-DI 07899878029267UDI-DIDate6 May 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number07899878029267 UDI-DI Date13 Dec 2022ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 987800049VV registered 6 May 2026 Active
  • FDA GUDID UDI-DI 07899878029267 listed 13 Dec 2022 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 07899878029267
  2. Registered EUDAMED 987800049VV

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  • Withdrawn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
Neodent
Generic name
Dental implant abutment trial
Device name
Abutments Try-in
Model / Ref / Catalog
Abutment, 114.784
Primary DI / UDI-DI
07899878029267
Basic UDI-DI
987800049VV
FDA product code
NDP
EMDN code
P01020180 Dental implants - accessories
GMDN term
Dental implant abutment trial
Device class
Class I
Regulation number
872.3980
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution
Size
Outer Diameter — 3.3 Millimeter
Height — 6 Millimeter
Height — 1.5 Millimeter

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Sterilise before useEUDAMED
Yes
GUDID
No

Registry differences

EUDAMED and FDA GUDID describe the same product (same UDI-DI) and state different values:

  • Sterilise before use UDI-DI 07899878029267: EUDAMED states Yes, FDA GUDID states No.

Manufacturer details

EUDAMED SRN
BR-MF-000014512
Authorised representative
Etkon GmbH DE-AR-000009335

Similar devices in this category

Other devices filed under DENTAL IMPLANTS - ACCESSORIES.

Other devices from JJGC Indústria e Comércio de Materiais Dentários S/A.

See all devices from JJGC Indústria e Comércio de Materiais Dentários S/A. →

Properties

  • Sterilise before use YesEUDAMEDNoGUDID
  • Reusable
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (18, all answered No)