# K031795: Reliant Laser System

- Pathway: 510(k) (Traditional)
- Applicant: Reliant Technologies, Inc.
- Decided: Nov 10, 2003 after 153 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: 5 generations back to K936109 (1994). 25 ancestors in all.
318 later devices descend from it; 6 cite it directly.
0 of 344 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K022060: Lumenis Ultrapulse Encore Carbon Dioxide Surgical Lasers and Delivery Device Accessories, Lumenis, Inc. (2002) Summary page 1.

## Most influential descendants
- K040617: Reliant Laser System II (2004), 316 descendants of its own
- K042319: Reliant Laser II System and Accessories (2005), 284 descendants of its own
- K060301: Palomar LUX1540 Handpiece (2006), 260 descendants of its own
- K061652: Palomar LUX1540 Handpiece (2007), 259 descendants of its own
- K060310: Fraxel II SR Laser System and Accessories (2006), 230 descendants of its own

## Indications for use
Dermatological procedures requiring the coagulation of soft tissue

Source page: https://510kreport.com/device/K031795
Methodology: https://510kreport.com/methodology