# K254220: Reusable 3 Button Fingerswitch Wand

- Pathway: 510(k) (Special)
- Applicant: Soniquence, LLC
- Decided: Jan 27, 2026 after 29 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: 8 generations back to K933157 (1994). 34 ancestors in all.
No later device cites it as a predicate yet.
0 of 35 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K183611: Soniquence RF Generator and Soniquence Electrodes, Soniquence, LLC (2019) Summary page 6.
- K212222: Soniquence Reusable 3 Button Fingerswitch Wand, Soniquence, LLC (2022) Summary page 6.

## Indications for use
The Soniquence Reusable 3 Button Fingerswitch Wand is designed to be used with a Soniquence RF Generator and Soniquence monopolar electrodes for resection, dissection, incision, and hemostasis in soft tissue surgical procedures

Source page: https://510kreport.com/device/K254220
Methodology: https://510kreport.com/methodology