# Aloka Co. Ltd USA

- Location (FDA's records): Wallingford, CT
- FDA decisions: 2 (2003–2004): 2 510(k) clearances
- Product codes: IYN (1), IYO (1)
- Predicates its devices cite: 6 (1 its own); citations of its devices by later devices: 8 (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
- Aloka Co., Ltd.: 5 (https://510kreport.com/company/aloka)

## Firms that cite its devices most
- Aloka Co., Ltd.: 2 (https://510kreport.com/company/aloka)
- Esaote, S.p.A.: 1 (https://510kreport.com/company/esaote)
- Hitachi Aloka Medical,Ltd. (Hitachi Aloka Medical: 1 (https://510kreport.com/company/hitachi-aloka-medical-hitachi-aloka-medical)
- Pie Medical: 1 (https://510kreport.com/company/pie-medical)
- Hitachi Aloka Medical, Ltd.: 1 (https://510kreport.com/company/hitachi-aloka-medical)
- Olympus Medical Systems Corp.: 1 (https://510kreport.com/company/olympus-medical-systems)

## Its most-cited devices
- K032875: Aloka Model SSD-5500 V6.0 Ultrasound System (2003), cited by 7
- K041916: Aloka SSD-Alpha 5 Ultrasound System (2004), cited by 1

## Recent decisions
- K041916: Aloka SSD-Alpha 5 Ultrasound System (Jul 30, 2004)
- K032875: Aloka Model SSD-5500 V6.0 Ultrasound System (Sep 30, 2003)

Source page: https://510kreport.com/company/aloka-co-usa