CL-DC20, CL-DC21
FDA 510(k) K093751 · Good Doctors Co., Ltd.
510(k) numberK093751
Submission
- Device name
- CL-DC20, CL-DC21
- Applicant
- Good Doctors Co., Ltd.
Greenwood Village, CO, US - Received
- December 7, 2009
- Decision date
- February 24, 2010
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) statement available from FDA
Other 510(k)s with product code EBZ
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K253131 | Curing Light (M-Cure 6)EBZ · Traditional | Guangzhou Rebornendo Medical Instrument Co., Ltd. | 06/18/2026SE |
| K253461 | Demi ProEBZ · Traditional | Meta Systems Co., Ltd. | 10/14/2025SE |
| K242386 | BluemoonEBZ · Traditional | Genoss Co., Ltd. | 05/05/2025SE |
| K243921 | LED Curing Lights (DB686 HALO)EBZ · Traditional | Foshan Coxo Medical Instrument Co., Ltd. | 04/11/2025SE |
| K250009 | LED Curing Light (C01-X, C02-X)EBZ · Traditional | Premium Plus (Dongguan) Limited | 04/10/2025SE |
| K241238 | LOOP LED Curing Light System (CLK01)EBZ · Traditional | Garrison Dental Solutions, LLC | 08/01/2024SE |
| K223414 | Curing Light, Model: MaxCure 9EBZ · Traditional | Guilin Refine Medical Instrument Co., Ltd. | 11/15/2023SE |
| K233518 | BASE290 LED Curing LightEBZ · Traditional | Handpiece Headquarters | 11/02/2023SE |
| K223507 | CL-DP40 (Drs Light PRIME), CL-DP40 (Drs Light CHOICE)EBZ · Traditional | Good Doctors Co., Ltd. | 08/04/2023SE |
| K223142 | Coltolux Comfort LED Curing LightEBZ · Traditional | Dent4you AG | 12/22/2022SE |
More from Dent4you AG
| 510(k) | Device | Decision |
|---|---|---|
| K223507 | CL-DP40 (Drs Light PRIME), CL-DP40 (Drs Light CHOICE)EBZ · Traditional | 08/04/2023SE |
| K183471 | IC-WHCD100 (Inspire)NBL · Traditional | 07/02/2020SE |
| K173157 | Dr's Light2EBZ · Traditional | 05/29/2018SE |
| K171867 | Drs Finder NEOLQY · Traditional | 03/30/2018SE |
| K151274 | Dr's FinderLQY · Traditional | 02/04/2016SE |
| K071908 | Doctor's Light LED Dental Curing LightEBZ · Traditional | 08/23/2007SE |
Questions and answers
When was CL-DC20, CL-DC21 cleared by the FDA?
CL-DC20, CL-DC21 (K093751) received a 510(k) decision of Substantially Equivalent on February 24, 2010, 79 days after the submission was received.
What is the product code of K093751?
The FDA product code is EBZ – Activator, Ultraviolet, For Polymerization, a Class II (moderate risk) device regulated under 21 CFR 872.6070.