# Biosonix, Ltd.

- Location (FDA's records): Kfar Saba, IL
- FDA decisions: 1 (2002–2002): 1 510(k) clearance
- Product codes: DPW (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: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Koven and Assoc., Inc.: 1 (https://510kreport.com/company/koven-and-assoc)
- Echocath, Inc.: 1 (https://510kreport.com/company/echocath)
- Sometec, Inc.: 1 (https://510kreport.com/company/sometec)

## Firms that cite its devices most
- Cardiosonix, Ltd.: 2 (https://510kreport.com/company/cardiosonix)
- Neoprobe Corp.: 1 (https://510kreport.com/company/neoprobe)

## Its most-cited devices
- K013803: Flowguard Device (2002), cited by 3

## Recent decisions
- K013803: Flowguard Device (Feb 13, 2002)

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