# Xanar, Inc.

- Location (FDA's records): Colorado Springs, CO
- FDA decisions: 12 (1983–1986): 12 510(k) clearances
- Product codes: GEX (6), LNK (1), FYD (1), EWG (1)
- 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
- Coherent Medical Group: 1 (https://510kreport.com/company/coherent-medical-group)
- Hogan & Hartson: 1 (https://510kreport.com/company/hogan-hartson)

## Its most-cited devices
- K853620: Model XA-50 - CO2 Surgical Laser (1986), cited by 1
- K861688: Xanar CO2 Surgical Laser System Model Xap-15 (1986), cited by 1

## Recent decisions
- K861688: Xanar CO2 Surgical Laser System Model Xap-15 (Oct 3, 1986)
- K852436: Ambulase (Apr 18, 1986)
- K860496: Model NY-110 for Upper & Lower (GU) & Pulmonary (Mar 14, 1986)
- K853620: Model XA-50 - CO2 Surgical Laser (Jan 24, 1986)
- K850804: CO 2 Surgical Laser System NA-30 (Aug 15, 1985)
- K850805: CO 2 Surgical Laser System Model NA-40 (Aug 15, 1985)
- K850818: CO 2 Surgical Laser System NA-120 (Aug 15, 1985)
- K844087: Xanar Model Xse-300 Smoke Evaculater (Feb 27, 1985)

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