# K171752: X-Surge

- Pathway: 510(k) (Special)
- Applicant: Genicon, Inc.
- Decided: Oct 17, 2017 after 126 days
- Product code: GEI (Electrosurgical, Cutting & Coagulation & Accessories)
- Device class: 2
- Regulation: 21 CFR 878.4400
- 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 K910831 (1991). 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)
- K061417: Genicon Disposable Electrosurgical Instrumentation, Model 533-005-910, Genicon (2006) Summary page 4.

## Most influential descendants
- K210569: Disposable Monopolar Laparoscopic Shafts and Reusable Handles (2021), 0 descendants of its own

## Indications for use
Endoscopic surgical procedures. It is a family of instruments which includes graspers, dissectors, and scissors, which are intended to be used to grasp, manipulate, cut, and cauterized soft tissue.

Source page: https://510kreport.com/device/K171752
Methodology: https://510kreport.com/methodology