# Imalux Corporation

- Location (FDA's records): Cleveland, OH
- FDA decisions: 2 (2004–2004): 2 510(k) clearances
- Product codes: NQQ (1), KKX (1)
- Predicates its devices cite: 3 (0 its own); citations of its devices by later devices: 3 (0 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Imalux Coporation: 1 (https://510kreport.com/company/imalux-coporation)
- CIVCO Medical Instruments Co., Inc.: 1 (https://510kreport.com/company/civco-medical-instruments)
- Vision-Sciences, Inc.: 1 (https://510kreport.com/company/vision-sciences)

## Firms that cite its devices most
- Ninepoint Medical, Inc.: 2 (https://510kreport.com/company/ninepoint-medical)
- Perimeter Medical Imaging, Inc.: 1 (https://510kreport.com/company/perimeter-medical-imaging)

## Its most-cited devices
- K042894: Imalux Niris Imaging System (2004), cited by 2
- K041077: Imalux Oct Probe Guide (2004), cited by 1

## Recent decisions
- K042894: Imalux Niris Imaging System (Nov 19, 2004)
- K041077: Imalux Oct Probe Guide (Jun 25, 2004)

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