# Lasermed, Inc.

- Location (FDA's records): Salt Lake City, UT
- FDA decisions: 7 (1983–1999): 7 510(k) clearances
- Names in FDA's records: Lasermed, Inc. (3); Lasermed Corp. (3); Lasermed (1)
- Product codes: GEX (4), HQE (1), HQF (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 1 (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
- Ics of North America, Inc.: 1 (https://510kreport.com/company/ics-of-north-america)

## Its most-cited devices
- K970637: Accucure 1000 (1997), cited by 1

## Recent decisions
- K992061: Pulstar (Jul 30, 1999)
- K970637: Accucure 1000 (Apr 2, 1997)
- K964486: Accucure 3000 (Feb 18, 1997)
- K943411: Accucure 3000 (Apr 25, 1995)
- K843594: Airvit Model 8500 (Apr 11, 1985)
- K833532: Oculase 514 Ophthalmic Argon Laser (Feb 4, 1984)
- K828583: Lasermed Oculase Argon Laser (Jan 14, 1983)

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