# Fisma, Inc.

- Location (FDA's records): Salt Lake City, UT
- FDA decisions: 4 (1996–2000): 4 510(k) clearances
- Product codes: GEX (4)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 3 (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
- Lumenis, Inc.: 1 (https://510kreport.com/company/lumenis)
- Asclepion-Meditec AG: 1 (https://510kreport.com/company/asclepion-meditec)
- Iridex Corp: 1 (https://510kreport.com/company/iridex)

## Its most-cited devices
- K990174: Atlas-Elite,Model E-80,Corium 200,Corium 400, Model E-90, Elite, Model E-80-II, Elite Ultra, Model E-80-IV (1999), cited by 3

## Recent decisions
- K000158: Veinlase, Model E50-K8-B5, Spectrum K8, Model E50-K8-B9 (Aug 24, 2000)
- K991464: Dental 200, Dental 300, Dental 400, Models E-20, E-60, E-50 (Jul 20, 1999)
- K990174: Atlas-Elite,Model E-80,Corium 200,Corium 400, Model E-90, Elite, Model E-80-II, Elite Ultra, Model E-80-IV (Apr 1, 1999)
- K963124: PC Laser with Smart Plug (PC Edo & Dental 200) (Nov 8, 1996)

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