# K151273: InMode FRF Applicator

- Pathway: 510(k) (Traditional)
- Applicant: Inmode MD, Ltd.
- Decided: Jan 4, 2016 after 236 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: 18 generations back to K943450 (1995). 257 ancestors in all.
3 later devices descend from it; 1 cites it directly.
0 of 261 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K130501: Intensif, Endymed Medical, Ltd. (2014) Summary page 4.

## Most influential descendants
- K221571: InMode Multi-system (2022), 2 descendants of its own
- K251632: Optimas MAX System (2025), 1 descendant of its own
- K252215: InbellaMAX System (2025), 0 descendants of its own

## Indications for use
The InMode FRF Applicator is intended for use in Dermatologic and General Surgical procedures for Electrocoagulation and Hemostasis. At higher energy levels greater than 62 m/pin, use of the FRF applicator is limited to Skin Types I-IV.

Source page: https://510kreport.com/device/K151273
Methodology: https://510kreport.com/methodology