# K993942: Litesaber 2000

- Pathway: 510(k) (Traditional)
- Applicant: Laser Dental Innovations
- Decided: Jan 18, 2000 after 60 days
- Product code: GEX (Powered Laser Surgical Instrument)
- Device class: 2
- Regulation: 21 CFR 878.4810
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 3 generations back to K953074 (1995). 3 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K971539: Novatip Family of Laser Handpiece Tips, Xanova Corp. (1997) Summary page 1.

## Most influential descendants
- K082445: CURATIVE980 Diode Laser (2008), 0 descendants of its own

## Indications for use
The LiteSaber™2000 indications for use are for the cleared indications for the laser system to which it is attached. For example, dermatological, ENT, general surgery, GYN surgery, oral/dental, maxillofacial, orthopaedic and podiatric procedures for the incision, excision, ablation, vaporization and hemostasis of soft tissue.

Source page: https://510kreport.com/device/K993942
Methodology: https://510kreport.com/methodology