# K172818: LMT-3000

- Pathway: 510(k) (Traditional)
- Applicant: Lameditech Co., Ltd.
- Decided: Mar 7, 2018 after 170 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: 2 generations back to K981746 (1998). 3 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K013021: Lightlance Laser Skin Perforator, Innotech USA, Inc. (2002) Summary page 5.

## Most influential descendants
- K241646: Ortiv (Ortiv-BL, Ortiv-WH) (2024), 0 descendants of its own

## Indications for use
The LMT-3000 is a portable, battery-operated laser lancing device indicated for obtaining capillary blood samples in both institutional and at-home settings.

Source page: https://510kreport.com/device/K172818
Methodology: https://510kreport.com/methodology