Dvi Curing Light

FDA 510(k) K043530 · Designs For Vision, Inc.

Substantially Equivalent

510(k) numberK043530

Submission

Device name
Dvi Curing Light
Applicant
Designs For Vision, Inc.
North Attleboro, MA, US
Received
December 21, 2004
Decision date
January 25, 2005
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

510(k)DeviceApplicantDecision
K253131Curing Light (M-Cure 6)EBZ · Traditional Guangzhou Rebornendo Medical Instrument Co., Ltd.06/18/2026SE
K253461Demi ProEBZ · Traditional Meta Systems Co., Ltd.10/14/2025SE
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

More from Dent4you AG

510(k)DeviceDecision
K051786Melide Fiberoptic LightFST · Special 08/15/2005SE
K032283Designs for Vision Fiberoptic LightGDB · Special 08/20/2003SE
K013880Daylite Xenon Light SourcesGCT · Traditional 12/07/2001SE
K801058Illuminated SpeculumFXF · Traditional 05/28/1980SE

Questions and answers

When was Dvi Curing Light cleared by the FDA?

Dvi Curing Light (K043530) received a 510(k) decision of Substantially Equivalent on January 25, 2005, 35 days after the submission was received.

What is the product code of K043530?

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