# Endosound, Inc.

- Location (FDA's records): Portland, OR
- FDA decisions: 2 (2023–2025): 2 510(k) clearances
- Product codes: ODG (1), ODC (1)
- Predicates its devices cite: 5 (0 its own); citations of its devices by later devices: 0 (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
- Olympus Medical Systems Corp.: 1 (https://510kreport.com/company/olympus-medical-systems)
- Hitachi Aloka Medical,Ltd. (Hitachi Aloka Medical: 1 (https://510kreport.com/company/hitachi-aloka-medical-hitachi-aloka-medical)
- Pentax of America, Inc.: 1 (https://510kreport.com/company/pentax-of-america)
- STERIS Corporation: 1 (https://510kreport.com/company/steris)
- Boston Scientific Corp: 1 (https://510kreport.com/company/boston-scientific)

## Recent decisions
- K250145: Biopsy Port Adapter (Oct 17, 2025)
- K232518: EndoSound Vision System; EVS (Dec 27, 2023)

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