# K041419: Lightforce LF 20/30 980NM Surgical Diode Laser System

- Pathway: 510(k) (Traditional)
- Applicant: Medical Energy, Inc.
- Decided: Aug 26, 2004 after 90 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
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names no predicate by number.

## Indications for use
For soft tissue Incision, Excision, Vaporization and Coagulation: * Gastroenterology * Neurology * General Surgery * Urology * Gynecology * Pulmonary * ENT/Head & Neck * Plastic Surgery Including: * Gynecology-Endometrial Ablation (K871512) * Urology Surgery (K871516) * Rectal Patho. & Hemorrhoid (K871514) * Gastro Intestinal Bleeding (K871515) * Palliation of Gastro Malignancies (K871513) * Pulmonary Obstructions (K871511A)

Source page: https://510kreport.com/device/K041419
Methodology: https://510kreport.com/methodology