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Diatech Diamond Instruments 211722DD

by Coltène/Whaledent AG

Diatech Diamond Instruments 211722DD (MX35-012-4-C) is a Class I device made by Coltène/Whaledent AG, listed in FDA GUDID since 14 Aug 2022 (UDI-DI J006211722DD0), 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 NumberJ006211722DD0 UDI-DI Date14 Aug 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  • Withdrawn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
Diatech Diamond Instruments
Generic name
Diamond dental bur, reusable
Model / Ref / Catalog
211722DD, MX35-012-4-C
Primary DI / UDI-DI
J006211722DD0
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

Related devices

Category: Diamond dental bur, reusable

Other devices from Coltène/Whaledent AG

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Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)