# Cruxell Corp.

- Location (FDA's records): Daejeon, KR
- FDA decisions: 2 (2019–2021): 2 510(k) clearances
- Product codes: MUH (2)
- Predicates its devices cite: 3 (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 whose devices it cites most
- Soredex Palodex Group OY: 1 (https://510kreport.com/company/soredex-palodex-group)
- Instrumentarium Dental, Palodex Group OY: 1 (https://510kreport.com/company/instrumentarium-dental-palodex-group)
- Orion Corporation Soredex: 1 (https://510kreport.com/company/orion-soredex)

## Firms that cite its devices most
- Genoray Co., Ltd.: 1 (https://510kreport.com/company/genoray)

## Its most-cited devices
- K183637: Cruxcan (CRX-1000) (2019), cited by 1

## Recent decisions
- K211317: Cruxview (Jul 29, 2021)
- K183637: Cruxcan (CRX-1000) (Feb 12, 2019)

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