Luxtron
Country not established
- Devices
- 4
What Luxtron makes
Luxtron manufactures fluoroptic-based medical devices for precise temperature monitoring, including multichannel thermometers and fluoroptic thermometry systems designed for clinical and research applications.
The company’s products are regulated as Class II devices under FDA 510(k) clearance requirements and are listed in the FDA’s 510(k) database. Luxtron is headquartered in the United States.
Catalogue
Biomedical Fluoroptic Ref K821070
510(k) 510(k)Luxtron Model 3100/3101/3102 Multichannel Ref K923189
510(k) 510(k)Multichannel 2000 Fluoroptic Thermomet Ref K841105
510(k) 510(k)Model 3000 Mlultichannel Fluoroptic Thermometer Ref K861623
510(k) 510(k)
Frequently asked questions
How many devices does Luxtron have in the registry?
The registry currently lists 4 devices for Luxtron. Devices recorded under merged duplicate company entries are counted once.
Which registries list Luxtron's devices?
Among its 4 most recently registered devices, Luxtron has devices listed in FDA 510(k) (4 devices).
What risk classes do Luxtron's devices fall under?
Among its 4 most recently registered devices, the classes recorded for Luxtron's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Luxtron in the registry?
The most recently registered devices listed for Luxtron include BIOMEDICAL FLUOROPTIC, LUXTRON MODEL 3100/3101/3102 MULTICHANNEL, MULTICHANNEL 2000 FLUOROPTIC THERMOMET and MODEL 3000 MLULTICHANNEL FLUOROPTIC THERMOMETER.