# American Laser Medical

- Location (FDA's records): Salt Lake City, UT
- FDA decisions: 5 (1996–1999): 5 510(k) clearances
- Product codes: GEX (5)
- Predicates its devices cite: 3 (1 its own); citations of its devices by later devices: 3 (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 whose devices it cites most
- Hgm Medical Laser Systems, Inc.: 1 (https://510kreport.com/company/hgm-medical-laser-systems)
- Metatech Corp.: 1 (https://510kreport.com/company/metatech)

## Firms that cite its devices most
- American Laser Corp.: 1 (https://510kreport.com/company/american-laser)
- Quantel Medical: 1 (https://510kreport.com/company/quantel-medical)

## Its most-cited devices
- K970667: Nuvo-Lase 660 Laser System (1997), cited by 2
- K972561: Nuvolase 660 Laser System for Ophthalmology (1997), cited by 1

## Recent decisions
- K990780: Nuvolase 532 Cutaneous Laser System (Mar 22, 1999)
- K972765: Nuvolase 720 System for Ophthalmology Laser (Oct 21, 1997)
- K972561: Nuvolase 660 Laser System for Ophthalmology (Oct 6, 1997)
- K970667: Nuvo-Lase 660 Laser System (May 13, 1997)
- K963389: Flex-Lase 600 Series Ion Laser System (Nov 26, 1996)

Source page: https://510kreport.com/company/american-laser-medical