# K163190: InMode RF System

- Pathway: 510(k) (Special)
- Applicant: Inmode MD, Ltd.
- Decided: Dec 12, 2016 after 28 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: 19 generations back to K943450 (1995). 105 ancestors in all.
No later device cites it as a predicate yet.
0 of 106 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K151793: InMode RF System, Inmode MD, Ltd. (2016) Summary page 5.

## 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/K163190
Methodology: https://510kreport.com/methodology