# K233921: Luvis Chair (LC700C)

- Pathway: 510(k) (Traditional)
- Applicant: Dentis Co., Ltd.
- Decided: Sep 6, 2024 after 268 days
- Product code: KLC (Chair, Dental, With Operative Unit)
- Device class: 1
- Regulation: 21 CFR 872.6250
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 4 generations back to K962071 (1996). 4 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K183347: K3, Osstem Implant Co., Ltd. (2019) Summary page 6.

## Most influential descendants
- K242611: Integral Dental Units (2025), 0 descendants of its own

## Indications for use
Luvis Chair is intended to supply power to and serve as a base for dental devices and accessories. This Device includes a dental chair and is intended for use in the dental clinic environment and is designed for use by trained dental professionals, dentists and/or dental assistants.

Source page: https://510kreport.com/device/K233921
Methodology: https://510kreport.com/methodology