# K121724: Endolight Led 1.1 Endolightled 1.2

- Pathway: 510(k) (Traditional)
- Applicant: Richard Wolf Medical Instruments Corp.
- Decided: Sep 20, 2012 after 100 days
- Product code: FCW (Light Source, Fiberoptic, Routine)
- Device class: 2
- Regulation: 21 CFR 876.1500
- 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 K961971 (1996). 6 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K983628: Xenon Light Source Auto Lip 5123, Model 2123.011, Richard Wolf Medical Instruments Corp. (1998) Summary page 1.
- K082813: Stryker Led Lightsource, Stryker Corp. (2008) Summary page 1.
- K102167: LO-50 Led Light Source, Fiberoptics Technology, Inc. (2010) Summary page 3.

## Most influential descendants
- K131226: Novaprobe Led Light Source (2014), 0 descendants of its own

## Indications for use
The ENDOLIGHT LED Light Source Projector is intended to be used to illuminate the surgical site during minimally invasive surgical procedures by producing light that is transmitted from the light source through fiber optic cable and a scope.

Source page: https://510kreport.com/device/K121724
Methodology: https://510kreport.com/methodology