# Surgilight, Inc.

- Location (FDA's records): Orlando, FL
- FDA decisions: 2 (2000–2002): 2 510(k) clearances
- Product codes: GEX (2)
- Predicates its devices cite: 2 (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 whose devices it cites most
- Avex Industries, Ltd.: 1 (https://510kreport.com/company/avex-industries)
- National Biological Corp.: 1 (https://510kreport.com/company/national-biological)

## Firms that cite its devices most
- Ra Medical Systems,Inc: 2 (https://510kreport.com/company/ra-medical-systems)

## Its most-cited devices
- K020973: EX-308 Excimer Laser for Phototherapy Treatment of Vitiligo (2002), cited by 1
- K993328: Surgilight, Inc Excimer Laser (2000), cited by 1

## Recent decisions
- K020973: EX-308 Excimer Laser for Phototherapy Treatment of Vitiligo (Mar 29, 2002)
- K993328: Surgilight, Inc Excimer Laser (Jul 18, 2000)

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