# Luxar Corp.

- Location (FDA's records): Bothell, WA
- FDA decisions: 17 (1988–1996): 17 510(k) clearances
- Product codes: GEX (17)
- Predicates its devices cite: 1 (1 its own); citations of its devices by later devices: 18 (1 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
- Clinicon Corp.: 4 (https://510kreport.com/company/clinicon)
- Diamond Age Systems, Inc.: 3 (https://510kreport.com/company/diamond-age-systems)
- Lightscalpel, LLC: 2 (https://510kreport.com/company/lightscalpel)
- Xanova Corp.: 1 (https://510kreport.com/company/xanova)
- Reliant Technologies, Inc.: 1 (https://510kreport.com/company/reliant-technologies)
- Omniguide Communications, Inc.: 1 (https://510kreport.com/company/omniguide-communications)
- Max Engineering, Ltd.: 1 (https://510kreport.com/company/max-engineering)
- Aesculight, LLC: 1 (https://510kreport.com/company/aesculight)

## Its most-cited devices
- K960475: Modified Luxar LX-20 Family CO2 Laser System (1996), cited by 8
- K953074: Modified Luxar LX-20 Family CO2 Laser System (1995), cited by 6
- K896478: Luxar Model LX-20 Minilase CO2 Laser (1990), cited by 3
- K903079: Endoguide (R), Microguide (TM), Flexiguide (TM) (1990), cited by 1

## Recent decisions
- K960475: Modified Luxar LX-20 Family CO2 Laser System (Apr 26, 1996)
- K953074: Modified Luxar LX-20 Family CO2 Laser System (Aug 28, 1995)
- K945888: Modified Luxar LX-20 Family C02 Laser System (Jan 27, 1995)
- K904068: Luxar Model LX-20 CO2 Laser (Apr 15, 1991)
- K903079: Endoguide (R), Microguide (TM), Flexiguide (TM) (Oct 4, 1990)
- K900066: Flexiguide (TM) CO2 Laser Hollow Flexible Fiber (Mar 19, 1990)
- K897040: Luxar Endoguide CO2 Laser Waveguide (Neuro.) (Feb 13, 1990)
- K896478: Luxar Model LX-20 Minilase CO2 Laser (Feb 8, 1990)

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