# K132771: Kingston Endoscopic Surgical Instruments

- Pathway: 510(k) (Traditional)
- Applicant: Qingdao Kingston Medical Devices, Ltd.
- Decided: Oct 28, 2014 after 418 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.
2 later devices descend from it; 1 cites it directly.
0 of 6 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
- K171825: Disposable Endoscopic Surgical Instrument, Reusable Endoscopic Surgical Instrument (2018), 1 descendant of its own
- K211019: Disposable Monopolar Laparoscopic Tips and Reusable Handles (2021), 0 descendants of its own

## Indications for use
Endoscopic Surgical Instruments are intended for cutting, grasping, dissecting and coagulation of soft tissue in endoscopic surgical procedures. They are intended for single patient use.

Source page: https://510kreport.com/device/K132771
Methodology: https://510kreport.com/methodology