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Horico F364

by Hopf, Ringleb & Co. GmbH & Cie.

Horico F364 is a Class I device made by Hopf, Ringleb & Co. GmbH & Cie., listed in FDA GUDID since 8 Jun 2023 (UDI-DI EHORF3648), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberEHORF3648 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  • Withdrawn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
F364
Primary DI / UDI-DI
EHORF3648
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

Similar devices

Other devices filed under FDA product code EHM (Strip, Polishing Agent).

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, all answered No)