# Lutech Industries, Inc.

- Location (FDA's records): Ronkonkoma, NY
- FDA decisions: 4 (2014–2017): 4 510(k) clearances
- Product codes: HEX (3), MWI (1)
- Predicates its devices cite: 1 (1 its own); citations of its devices by later devices: 1 (1 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Its most-cited devices
- K143119: LT-300 Video Colposcope (2014), cited by 1

## Recent decisions
- K170446: LT-300 SD Digital Video Colposcope (May 21, 2017)
- K160380: LT-300 HD (May 13, 2016)
- K150691: Datalys Multi-Parameter Patient Monitor (May 15, 2015)
- K143119: LT-300 Video Colposcope (Dec 18, 2014)

Source page: https://510kreport.com/company/lutech-industries