# Heartforce Medical, Inc.

- Location (FDA's records): Appollo Beach, FL
- FDA decisions: 1 (2009–2009): 1 510(k) clearance
- Product codes: DXR (1)
- Predicates its devices cite: 1 (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 whose devices it cites most
- Seismed Instruments, Inc.: 1 (https://510kreport.com/company/seismed-instruments)

## Firms that cite its devices most
- Cardiosense, Inc.: 1 (https://510kreport.com/company/cardiosense)
- Corsens Medical, Ltd.: 1 (https://510kreport.com/company/corsens-medical)
- Cardio-Phoenix, Inc.: 1 (https://510kreport.com/company/cardio-phoenix)

## Its most-cited devices
- K081603: Digital Ballistocardiograph, Model DGB 300 (2009), cited by 3

## Recent decisions
- K081603: Digital Ballistocardiograph, Model DGB 300 (Jul 24, 2009)

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