# Resoundant, Inc.

- Location (FDA's records): Rochester, MN
- FDA decisions: 2 (2019–2020): 2 510(k) clearances
- Product codes: LLZ (1), LNH (1)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 1 (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
- GE Medical Systems: 2 (https://510kreport.com/company/ge-medical-systems)

## Firms that cite its devices most
- Quality Electrodynamics, LLC: 1 (https://510kreport.com/company/quality-electrodynamics)

## Its most-cited devices
- K201389: Resoundant Acoustic Driver System (2020), cited by 1

## Recent decisions
- K201389: Resoundant Acoustic Driver System (Jul 10, 2020)
- K183193: MREplus+ Software (Aug 1, 2019)

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