# K182325: InMode RF System

- Pathway: 510(k) (Special)
- Applicant: Inmode MD, Ltd.
- Decided: Sep 26, 2018 after 30 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: 1 generation back to K171593 (2017). 1 ancestor in all.
14 later devices descend from it; 2 cite it directly.
0 of 16 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K171593: InMode RF System, Inmode MD, Ltd. (2017) Summary page 4.

## Most influential descendants
- K201150: InMode RF Multi-System (2020), 8 descendants of its own
- K210492: InMode RF Pro System (2021), 7 descendants of its own
- K233642: InMode RF System (2024), 4 descendants of its own
- K240780: InMode RF System (2024), 3 descendants of its own
- K221571: InMode Multi-system (2022), 2 descendants of its own

## Indications for use
The InMode RF System is indicated for use in dermatological and general surgical procedures for electro-coagulation and hemostasis

Source page: https://510kreport.com/device/K182325
Methodology: https://510kreport.com/methodology