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Denfinity 10.154.3118C

by 3R - Industria E Comercio Eireli

Denfinity 10.154.3118C is a Class I device made by 3R - Industria E Comercio Eireli, listed in FDA GUDID since 9 Mar 2026 (UDI-DI 07908738727080), 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 Number07908738727080 UDI-DI Date9 Mar 2026ListedStatusListed 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  • Withdrawn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
Denfinity
Generic name
Diamond dental bur, reusable
Model / Ref / Catalog
10.154.3118C
Primary DI / UDI-DI
07908738727080
FDA product code
EJL
GMDN term
Diamond dental bur, reusable
Device class
Class I
Regulation number
872.3240
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

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Properties

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