# K001719: Q-Lux Plasma 100 Light Cure Unit

- Pathway: 510(k) (Traditional)
- Applicant: Rolence Enterprise Co., Ltd.
- Decided: Oct 10, 2000 after 127 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
No predicates in its family tree.
2 later devices descend from it; 1 cites it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K033795: Plasmacure Bxe (2003), 1 descendant of its own
- K081287: Sapphire Plasma Arc Dental Curing Light (2008), 0 descendants of its own

Source page: https://510kreport.com/device/K001719
Methodology: https://510kreport.com/methodology