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Nti H7-008-Hp

by NTI - Kahla GmbH Rotary Dental Instruments

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 NumberE310H7008HP1 UDI-DI Date1 Jan 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  • Withdrawn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
Nti
Generic name
Carbide dental bur, reusable
Model / Ref / Catalog
H7-008-HP, H7-008HP
Primary DI / UDI-DI
E310H7008HP1
FDA product code
EJL
GMDN term
Carbide dental bur, reusable
Device class
Class I
Regulation number
872.3240
GUDID distribution status
In Commercial Distribution

Related devices

Category: Carbide dental bur, reusable

Other devices from NTI - Kahla GmbH Rotary Dental Instruments

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Properties

  • Premarket exempt
  • Lot / batch number
  • Manufacturing date

Other properties (12)

  • Supplied sterile: No
  • Sterilise before use: No
  • Single use: No
  • Implantable: No
  • Contains latex: No
  • Prescription use: No
  • Over-the-counter: No
  • Convenience kit: No
  • Combination product: No
  • HCT/P: No
  • Serial number: No
  • Expiration date: No