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Neodent 109.487

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

Neodent 109.487 is a Class II device made by JJGC Indústria e Comércio de Materiais Dentários S/A., listed in FDA GUDID since 22 Sep 2015 (UDI-DI 07898237567532), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number07898237567532 UDI-DI Date22 Sep 2015ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Neodent
Generic name
Orthodontic anchoring screw
Model / Ref / Catalog
109.487
Primary DI / UDI-DI
07898237567532
FDA product code
OAT
GMDN term
Orthodontic anchoring screw
Device class
Class II
Regulation number
872.3640
GUDID distribution status
In Commercial Distribution
Size
Outer Diameter — 1.3 Millimeter
Length — 7 Millimeter

Similar devices in this category

Other devices filed under Orthodontic anchoring screw.

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

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Properties

  • Supplied sterile
  • Single use
  • Implantable
  • Prescription use
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (8, all answered No)