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KOMET Dental Diamond Instruments KP6830L.315.014.A2

by Gebr. Brasseler GmbH & Co. KG

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberE226100175901 UDI-DI Date28 Apr 2023ListedStatusListed 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  • Withdrawn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
KOMET Dental Diamond Instruments
Generic Name
Diamond dental bur, reusable
Model / Ref / Catalog
KP6830L.315.014.A2, KP6830L.315.014
Primary DI / UDI-DI
E226100175901
FDA Product Code
DZP
GMDN Term
Diamond dental bur, reusable
Device Class
Class I
Regulation Number
872.4535
GUDID distribution status
In Commercial Distribution
Sterilization Method
Moist Heat or Steam Sterilization

Related devices

Category: Diamond dental bur, reusable

Other devices from Gebr. Brasseler GmbH & Co. KG

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Properties

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

Other properties (10)

  • 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
  • Expiration Date: No