# Futrex, Inc.

- Location (FDA's records): Gaithersburg, MD
- FDA decisions: 4 (1995–2015): 4 510(k) clearances
- Product codes: DSB (2), MNW (1), DXN (1)
- Predicates its devices cite: 3 (1 its own); citations of its devices by later devices: 2 (1 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
- Xperex Corporation: 1 (https://510kreport.com/company/xperex)
- Omron Healthcare, Inc.: 1 (https://510kreport.com/company/omron-healthcare)

## Firms that cite its devices most
- Fasstech: 1 (https://510kreport.com/company/fasstech)

## Its most-cited devices
- K963271: Futrex-6100/XL (1998), cited by 2

## Recent decisions
- K143108: HealthGuard-15 (Mar 27, 2015)
- K963271: Futrex-6100/XL (Aug 19, 1998)
- K922601: Futrex-5000A (Dec 28, 1995)
- K922600: Futrex-5000 (Dec 28, 1995)

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