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ComfiJect DN-30XS

by 3D Dental Designs and Development, LLC

ComfiJect DN-30XS is a Class I device made by 3D Dental Designs and Development, LLC, listed in FDA GUDID since 16 Dec 2022 (UDI-DI 00817169024132), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00817169024132 UDI-DI Date16 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  • Withdrawn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
ComfiJect
Generic name
Dental syringe needle, single-use
Model / Ref / Catalog
DN-30XS
Description
Essentials Premium Dental Needles 30G X 12mm EXTRA SHORT 0.3 X 12mm )
Primary DI / UDI-DI
00817169024132
FDA product code
DZM
GMDN term
Dental syringe needle, single-use
Device class
Class I
Regulation number
872.4730
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Dental syringe needle, single-use

Other devices from 3D Dental Designs and Development, LLC

See all devices from 3D Dental Designs and Development, LLC →

Properties

  • Supplied sterile
  • Sterilise before use
  • Single use
  • Premarket exempt
  • Lot / batch number
Other properties (10, all answered No)