Skip to content

FG diamond 533114

by DFS - DIAMON GmbH

FG diamond 533114 is a Class I device made by DFS - DIAMON GmbH, listed in FDA GUDID since 31 Dec 2020 (UDI-DI 04057176160140), 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 Number04057176160140 UDI-DI Date31 Dec 2020ListedStatusListed 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  • Withdrawn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
FG diamond
Generic name
Diamond dental bur, reusable
Model / reference
533114
Primary DI / UDI-DI
04057176160140
FDA product code
DZP
GMDN term
Diamond dental bur, reusable
Device class
Class I
Regulation number
872.4535
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Similar devices in this category

Other devices filed under Diamond dental bur, reusable.

Other devices from DFS - DIAMON GmbH

See all devices from DFS - DIAMON GmbH →

Properties

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