# K122875: Oricare L2700

- Pathway: 510(k) (Traditional)
- Applicant: Oricare, Inc.
- Decided: Dec 18, 2012 after 90 days
- Product code: FSY (Light, Surgical, Ceiling Mounted)
- Device class: 2
- Regulation: 21 CFR 878.4580
- 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 K965130 (1997). 8 ancestors in all.
No later device cites it as a predicate yet.
0 of 9 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K070442: Powerled Surgical Light System, Maquet S.A. (2007) Summary page 1.
- K072072: Harmony Led-1 Surgical Lighting System, STERIS Corporation (2007) Summary page 1.

## Indications for use
The Oricare L2700 Series Surgical Lamps provide illumination at varying illumination levels to the patient surgical area and provide video-visual procedural support for medical staff during surgical procedures.

Source page: https://510kreport.com/device/K122875
Methodology: https://510kreport.com/methodology