# K141904: Viora V-Touch

- Pathway: 510(k) (Traditional)
- Applicant: Viora, Ltd.
- Decided: Oct 21, 2014 after 99 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: 16 generations back to K943450 (1995). 65 ancestors in all.
No later device cites it as a predicate yet.
0 of 66 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K090221: Reaction System, Viora, Ltd. (2009) Summary page 4.

## Indications for use
The V-Touch is intended for dermatological procedures. The ST applicator is indicated for the treatment of relief of minor muscle aches and pain, relief of muscle spasm and temporary improvement of local blood circulation.

Source page: https://510kreport.com/device/K141904
Methodology: https://510kreport.com/methodology