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Neodent 125.124

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

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number07899878029670 UDI-DI Date13 Dec 2022ListedStatusListed GUDID: in commercial distribution

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  • Withdrawn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, reusable
Model / Ref / Catalog
125.124
Primary DI / UDI-DI
07899878029670
FDA Product Code
NDP
GMDN Term
Surgical drill guide, reusable
Device Class
Class I
Regulation Number
872.3980
GUDID distribution status
In Commercial Distribution
Size
Outer Diameter — 3.75 Millimeter
Outer Diameter — 3.5 Millimeter

Related devices

Category: Surgical drill guide, reusable

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

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Properties

  • Prescription Use
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (9)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No