Valiant Curing Light

FDA 510(k) K170101 · Inter-Med/Vista Dental Products

Substantially Equivalent

510(k) numberK170101

Submission

Device name
Valiant Curing Light
Applicant
Inter-Med/Vista Dental Products
Racine, WI, US
Received
January 11, 2017
Decision date
June 8, 2017
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
EBZ – Activator, Ultraviolet, For Polymerization
Device class
Class II (moderate risk)
Regulation
21 CFR 872.6070
Specialty
Dental

Other 510(k)s with product code EBZ

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K242386BluemoonEBZ · Traditional Genoss Co., Ltd.05/05/2025SE
K243921LED Curing Lights (DB686 HALO)EBZ · Traditional Foshan Coxo Medical Instrument Co., Ltd.04/11/2025SE
K250009LED Curing Light (C01-X, C02-X)EBZ · Traditional Premium Plus (Dongguan) Limited04/10/2025SE
K241238LOOP™ LED Curing Light System (CLK01)EBZ · Traditional Garrison Dental Solutions, LLC08/01/2024SE
K223414Curing Light, Model: MaxCure 9EBZ · Traditional Guilin Refine Medical Instrument Co., Ltd.11/15/2023SE
K233518BASE290 LED Curing LightEBZ · Traditional Handpiece Headquarters11/02/2023SE
K223507CL-DP40 (Dr’s Light PRIME), CL-DP40 (Dr’s Light CHOICE)EBZ · Traditional Good Doctors Co., Ltd.08/04/2023SE
K223142Coltolux Comfort LED Curing LightEBZ · Traditional Dent4you AG12/22/2022SE

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Questions and answers

When was Valiant Curing Light cleared by the FDA?

Valiant Curing Light (K170101) received a 510(k) decision of Substantially Equivalent on June 8, 2017, 148 days after the submission was received.

What is the product code of K170101?

The FDA product code is EBZ – Activator, Ultraviolet, For Polymerization, a Class II (moderate risk) device regulated under 21 CFR 872.6070.