# K171344: Xenocor Xenoscope Laparoscopic System

- Pathway: 510(k) (Special)
- Applicant: Xenocor, Inc.
- Decided: Jun 1, 2017 after 24 days
- Product code: GCJ (Laparoscope, General & Plastic Surgery)
- 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: 3 generations back to K923982 (1993). 5 ancestors in all.
No later device cites it as a predicate yet.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K161838: Xenocor Xenoscope Laparoscopic System, Xenocor, Inc. (2016) Summary page 4.

## Indications for use
The Xenoscope™ is intended to be used in diagnostic and therapeutic procedures for endoscopy and endoscopic surgery within the thoracic and peritoneal cavities including the female reproductive organs.

Source page: https://510kreport.com/device/K171344
Methodology: https://510kreport.com/methodology