# K123682: Inmode Hair Removal (HR) Device

- Pathway: 510(k) (Traditional)
- Applicant: Inmode MD, Ltd.
- Decided: Feb 27, 2013 after 89 days
- Product code: GEX (Powered Laser Surgical Instrument)
- Device class: 2
- Regulation: 21 CFR 878.4810
- 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). 223 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 225 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K001746: Lightsheer Pulsed Diode Array Laser System (Family of Products), Coherent Star (2000) Summary page 3.
- K090762: LEDA, Quantel Derma GmbH (2009) Summary page 1.

## Most influential descendants
- K142952: InMode Diolaze Device (2015), 0 descendants of its own

## Indications for use
The InMode Hair Removal (HR) device is indicated for use for hair removal.

Source page: https://510kreport.com/device/K123682
Methodology: https://510kreport.com/methodology