# K212561: MTX-C1

- Pathway: 510(k) (Traditional)
- Applicant: Ilooda Co,., Ltd.
- Decided: Sep 27, 2022 after 410 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: 17 generations back to K943450 (1995). 66 ancestors in all.
No later device cites it as a predicate yet.
0 of 67 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K143554: Venus Legacy CX, Venus Concept, Ltd. (2015) Summary page 4.

## Indications for use
The MTX-C1 is intended for the treatment of the following medical condition; using three types of handpieces for delivery of non-thermal RF combined with massage: Relief of minor muscle aches and pain, relief of muscle spasm Temporary improvement of local blood circulation Temporary reduction in the appearance of cellulite

Source page: https://510kreport.com/device/K212561
Methodology: https://510kreport.com/methodology