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Horico F374LW

by Hopf, Ringleb & Co. GmbH & Cie.

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 NumberEHORF374LW8 UDI-DI Date8 Jun 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  • Withdrawn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
Dental abrasive strip, single-use
Model / reference
F374LW
Primary DI / UDI-DI
EHORF374LW8
FDA product code
EHM
GMDN term
Dental abrasive strip, single-use
Device class
Class I
Regulation number
872.6010
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Dental abrasive strip, single-use

Other devices from Hopf, Ringleb & Co. GmbH & Cie.

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

Properties

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

Other properties (9)

  • Supplied sterile: 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