# Mutoh America Co., Ltd.

- Location (FDA's records): Deer Field, IL
- FDA decisions: 1 (2001–2001): 1 510(k) clearance
- Product codes: LFL (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 5 (0 its own)
- Recalls linked to its devices: 4 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Integra Neurosciences: 2 (https://510kreport.com/company/integra-neurosciences)
- Olympus Optical Co., Ltd.: 1 (https://510kreport.com/company/olympus-optical)
- Katalyst Surgical, LLC: 1 (https://510kreport.com/company/katalyst-surgical)
- Aomori Olympus Co., Ltd.: 1 (https://510kreport.com/company/aomori-olympus)

## Its most-cited devices
- K010309: Sonopet Model Ust-2001 Ultrasonic Surgical Aspirator (2001), cited by 5

## Recent decisions
- K010309: Sonopet Model Ust-2001 Ultrasonic Surgical Aspirator (Apr 18, 2001)

Source page: https://510kreport.com/company/mutoh-america