L3 Light Guide

FDA UDI

Class II (US FDA UDI)

by Bonart Co., Ltd.

Identity

Trade Name: L3 LIGHT GUIDE FDA UDI
Generic Name: Dental laboratory curing unit FDA UDI
Model / Reference: LD1009-171 FDA UDI

Identifiers

Primary DI / UDI-DI: 04719873120567 FDA UDI
510(k) Number: K062289 FDA UDI
FDA Product Code: EBZ FDA UDI
GMDN Term: Dental laboratory curing unit FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 872.6070 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Dental laboratory curing unit

L3 Light Guide by Bonart Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental laboratory curing unit.

First Medica — USA THINK INC. · Class II
Biohazard Shipping Pouch — Hager Worldwide, Inc. · Class I
Paradigm™ DeepCure — 3M Deutschland GmbH · Class II
Black Gasket for 6/8 qt.Pressure Pot — Hager Worldwide, Inc. · Class I
Slimax-C Plus — Beyes Dental Canada Inc · Class II
Elipar™ Freelight™ — 3M Deutschland GmbH · Class II
Elipar™ DeepCure-S — 3M Deutschland GmbH · Class II
Safco Influx LED Curing Light — Safco Dental Supply · Class II

Cleared under the same submission

K062289 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Bonart Co., Ltd.

Sources (1)

FDA UDI 2774f446-19da-4a5d-b04b-40d6fef5f8ea 33 fields · synced May 30, 2026