# Luxtron

- Location (FDA's records): Mchenry, IL
- FDA decisions: 4 (1982–1994): 4 510(k) clearances
- Product codes: FLL (4)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 2 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Vivant Medical, Inc.: 1 (https://510kreport.com/company/vivant-medical)
- Invivo Research, Inc.: 1 (https://510kreport.com/company/invivo-research)

## Its most-cited devices
- K841105: Multichannel 2000 Fluoroptic Thermomet (1984), cited by 1
- K923189: Luxtron Model 3100/3101/3102 Multichannel (1994), cited by 1

## Recent decisions
- K923189: Luxtron Model 3100/3101/3102 Multichannel (Mar 28, 1994)
- K861623: Model 3000 Mlultichannel Fluoroptic Thermometer (Aug 19, 1986)
- K841105: Multichannel 2000 Fluoroptic Thermomet (Jul 3, 1984)
- K821070: Biomedical Fluoroptic (Jul 13, 1982)

Source page: https://510kreport.com/company/luxtron