# Acculaser, Inc.

- Location (FDA's records): Chevy Chase, MD
- FDA decisions: 2 (2002–2004): 2 510(k) clearances
- Product codes: NHN (2)
- Predicates its devices cite: 3 (1 its own); citations of its devices by later devices: 6 (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
- Microlight Corporation of America: 2 (https://510kreport.com/company/microlight-of-america)

## Firms that cite its devices most
- Grt Solutions, Inc.: 1 (https://510kreport.com/company/grt-solutions)
- Medical Laser Systems, Inc.: 1 (https://510kreport.com/company/medical-laser-systems)
- Texas Applied Biomedical Services: 1 (https://510kreport.com/company/texas-applied-biomedical-services)
- Thor Intl.: 1 (https://510kreport.com/company/thor-intl)
- Advanced Medical Technologies AG: 1 (https://510kreport.com/company/advanced-medical-technologies)

## Its most-cited devices
- K020657: Acculaser Pro Low Level Laser Therapy Device (2002), cited by 5
- K023060: Acculaser PRO4 (2004), cited by 1

## Recent decisions
- K023060: Acculaser PRO4 (Mar 19, 2004)
- K020657: Acculaser Pro Low Level Laser Therapy Device (Jul 29, 2002)

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