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Neodent 127.011

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

Neodent 127.011 is a Class I device made by JJGC Indústria e Comércio de Materiais Dentários S/A., listed in FDA GUDID since 13 Dec 2022 (UDI-DI 07899878010685), 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 Number07899878010685 UDI-DI Date13 Dec 2022ListedStatusListed 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  • Withdrawn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
Manual bone mill
Model / Ref / Catalog
127.011
Primary DI / UDI-DI
07899878010685
FDA product code
LYS
GMDN term
Manual bone mill
Device class
Class I
Regulation number
888.4540
GUDID distribution status
In Commercial Distribution

Related devices

Category: Manual bone mill

Similar devices in this category

Other devices filed under Manual bone mill.

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

  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (10, all answered No)