Skip to content

Neodent 125.194

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

Neodent 125.194 is a Class I device made by JJGC Indústria e Comércio de Materiais Dentários S/A., listed in FDA GUDID since 27 May 2025 (UDI-DI 07899878063414), 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 Number07899878063414 UDI-DI Date27 May 2025ListedStatusListed 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  • Withdrawn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
Surgical drill guide, single-use
Model / Ref / Catalog
125.194
Primary DI / UDI-DI
07899878063414
FDA product code
NDP
GMDN term
Surgical drill guide, single-use
Device class
Class I
Regulation number
872.3980
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization
Size
Outer Diameter — 4.0 Millimeter

Related devices

Category: Surgical drill guide, single-use

Similar devices in this category

Other devices filed under Surgical drill guide, single-use.

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