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Horico Fg 166G018

by Hopf, Ringleb & Co. GmbH & Cie. 2 variants

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 NumberEHORFG166G0182 UDI-DI Date5 Jul 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  • Withdrawn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
Horico
Generic name
Diamond dental bur, reusable
Model / reference
FG 166G018
Primary DI / UDI-DI
EHORFG166G0182
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 Hopf, Ringleb & Co. GmbH & Cie.

See all devices from Hopf, Ringleb & Co. GmbH & Cie. →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date

Other properties (10)

  • Supplied 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