# K071908: Doctor's Light Led Dental Curing Light

- Pathway: 510(k) (Traditional)
- Applicant: Good Doctors Co., Ltd.
- Decided: Aug 23, 2007 after 44 days
- Product code: EBZ (Activator, Ultraviolet, For Polymerization)
- Device class: 2
- Regulation: 21 CFR 872.6070
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K033520 (2003). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K033520: Bluephase, Ivoclar Vivadent, Inc. (2003) Summary page 1.
- (no number) Turbo-Pen: named in the summary without a submission number

## Indications for use
Curing of dental composites using visible light.

Source page: https://510kreport.com/device/K071908
Methodology: https://510kreport.com/methodology