# Vios Medical, Inc.

- Location (FDA's records): St. Paul, MN
- FDA decisions: 3 (2015–2018): 3 510(k) clearances
- Product codes: DRT (2), DXJ (1)
- Predicates its devices cite: 6 (1 its own); citations of its devices by later devices: 7 (1 its own)
- Recalls linked to its devices: 4 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Sotera Wireless, Inc.: 2 (https://510kreport.com/company/sotera-wireless)
- Vitalconnect, Inc.: 1 (https://510kreport.com/company/vitalconnect)
- GE Healthcare: 1 (https://510kreport.com/company/ge-healthcare)
- Nonin Medical, Inc.: 1 (https://510kreport.com/company/nonin-medical)

## Firms that cite its devices most
- Murata Vios, Inc.: 4 (https://510kreport.com/company/murata-vios)
- Hmicro, Inc.: 1 (https://510kreport.com/company/hmicro)
- Caretaker Medical, LLC: 1 (https://510kreport.com/company/caretaker-medical)

## Its most-cited devices
- K150992: Vios Monitoring System (2015), cited by 3
- K173107: Vios Central Station Monitor Software, Vios Central Server Software (2018), cited by 2
- K172586: Vios Monitoring System™ Model 2050 (2018), cited by 2

## Recent decisions
- K173107: Vios Central Station Monitor Software, Vios Central Server Software (Jul 26, 2018)
- K172586: Vios Monitoring System™ Model 2050 (Jun 22, 2018)
- K150992: Vios Monitoring System (Dec 16, 2015)

Source page: https://510kreport.com/company/vios-medical