HORICO AuFG540c008

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

HORICO AuFG540c008 is a Class I device made by Hopf, Ringleb & Co. GmbH & Cie., listed in FDA GUDID since 30 Jun 2023 (UDI-DI EHORAUFG540C0082), 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

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	NumberEHORAUFG540C0082 UDI-DI	Date30 Jun 2023Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Horico
Generic name: Diamond dental bur, reusable
Model / reference: AuFG540c008

Primary DI / UDI-DI: EHORAUFG540C0082
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

Similar devices in this category

Other devices filed under Diamond dental bur, reusable.

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

Horico Fg 299X018

Class I
Horico F364

Class I
Horico Fg 005 018

Class I
HORICO AuFG166 010

Class I

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, all answered No)