# K212222: Soniquence Reusable 3 Button Fingerswitch Wand

- Pathway: 510(k) (Special)
- Applicant: Soniquence, LLC
- Decided: Sep 2, 2022 after 413 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: 7 generations back to K933157 (1994). 33 ancestors in all.
1 later device descends from it; 1 cites it directly.
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 5.

## Most influential descendants
- K254220: Reusable 3 Button Fingerswitch Wand (2026), 0 descendants of its own

## 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/K212222
Methodology: https://510kreport.com/methodology