# K090025: Matrix RF Applicator

- Pathway: 510(k) (Traditional)
- Applicant: Syneron Medical, Ltd.
- Decided: Jan 8, 2010 after 368 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). 252 ancestors in all.
18 later devices descend from it; 4 cite it directly.
0 of 271 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K073572: Matrix RF Applicator, Syneron Medical, Ltd. (2008) Summary page 1.
- K052936: Thermage Thermacool System, Thermage, Inc. (2007) Summary page 1.
- K070004: Accent, Alma Lasers, Ltd. (2007) Summary page 1.

## Most influential descendants
- K180359: BTL-FR2000 (2018), 9 descendants of its own
- K193201: BTL-785F (2020), 8 descendants of its own
- K211639: BTL-785W (2022), 7 descendants of its own
- K222556: BTL-785X (2023), 5 descendants of its own
- K233604: BTL-785S (2024), 3 descendants of its own

## Indications for use
The Matrix RF Applicator is intended for dermatological procedures requiring ablation and resurfacing of the skin, and for the treatment of facial wrinkles.

Source page: https://510kreport.com/device/K090025
Methodology: https://510kreport.com/methodology