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Neodent 110.159

by JJGC Indústria e Comércio de Materiais Dentários S/A.

Part of a family of 13 devices: see the family page

Ref 110.159Model Instrument

Neodent 110.159 is a Class I device made by JJGC Indústria e Comércio de Materiais Dentários S/A., registered in EUDAMED on 8 May 2026 (Basic UDI-DI 987800063VP) and listed in FDA GUDID since 12 Dec 2022 (UDI-DI 07899878001133), 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 Number987800063VP Basic UDI-DI 07899878001133UDI-DIDate8 May 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number07899878001133 UDI-DI Date12 Dec 2022ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 987800063VP registered 8 May 2026 Active
  • FDA GUDID UDI-DI 07899878001133 listed 12 Dec 2022 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 07899878001133
  2. Registered EUDAMED 987800063VP

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  • Withdrawn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 osteotome
Device name
Instruments for Bone Grafting and Sinus Lift
Model / Ref / Catalog
110.159, Instrument
Primary DI / UDI-DI
07899878001133
Basic UDI-DI
987800063VP
FDA product code
EMM
EMDN code
Z12139099 Various orthopaedic and traumatology instruments - other
GMDN term
Dental osteotome
Device class
Class I
Regulation number
872.4565
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution
Size
Outer Diameter — 4.5 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 07899878001133: EUDAMED states Yes, FDA GUDID states No.

Related devices

Category: Dental osteotome

Similar devices in this category

Other devices filed under VARIOUS ORTHOPAEDIC AND TRAUMATOLOGY INSTRUMENTS - OTHER.

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)