Palmlight
FDA 510(k) K020057 · CAO Group, Inc.
510(k) numberK020057
Submission
- Device name
- Palmlight
- Applicant
- CAO Group, Inc.
Sandy, UT, US - Received
- January 8, 2002
- Decision date
- August 27, 2002
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary 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 |
|---|---|---|
| K254197 | Picasso Pro Diode Laser (002-00460)GEX · Traditional | 03/11/2026SE |
| K201904 | Monet Curing LaserQNF · Traditional | 11/24/2020SE |
| K201475 | Ultimate Contour, Ultimate Contour MiniPBX · Traditional | 10/28/2020SE |
| K181614 | Sterling Supreme Diode LaserGEX · Traditional | 09/10/2019SE |
| K181602 | Pioneer Elite Diode LaserGEX · Traditional | 09/10/2019SE |
| K181601 | Precise SHP Diode LaserGEX · Traditional | 09/09/2019SE |
| K171052 | Ultimate Contour, Ultimate Contour MiniPBX · Traditional | 10/20/2017SE |
| K171986 | Sterling Supreme Diode LaserGEX · Traditional | 09/22/2017SE |
| K160413 | Sterling 5W Diode LaserGEX · Traditional | 09/21/2016SE |
| K150585 | Ascent 3DEBZ · Abbreviated | 12/31/2015SE |
Questions and answers
When was Palmlight cleared by the FDA?
Palmlight (K020057) received a 510(k) decision of Substantially Equivalent on August 27, 2002, 231 days after the submission was received.
What is the product code of K020057?
The FDA product code is EBZ – Activator, Ultraviolet, For Polymerization, a Class II (moderate risk) device regulated under 21 CFR 872.6070.