# Sonostik, LLC

- Location (FDA's records): Canfield, OH
- FDA decisions: 2 (2015–2024): 2 510(k) clearances
- Product codes: DYB (2)
- Predicates its devices cite: 3 (1 its own); citations of its devices by later devices: 1 (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
- Terumo Medical Corp.: 1 (https://510kreport.com/company/terumo-medical)
- Techdevice Corporation: 1 (https://510kreport.com/company/techdevice)

## Its most-cited devices
- K152177: SonoStik IV Guide Wire Introducer (2015), cited by 1

## Recent decisions
- K243061: SonoStik Guide Wire Introducer (Nov 4, 2024)
- K152177: SonoStik IV Guide Wire Introducer (Oct 1, 2015)

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