# Aomori Olympus Co., Ltd.

- Location (FDA's records): Melville, NY
- FDA decisions: 7 (2003–2005): 7 510(k) clearances
- Product codes: LFL (4), FGE (2), EOQ (1)
- Predicates its devices cite: 26 (4 its own); citations of its devices by later devices: 9 (4 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 Optical Co., Ltd.: 12 (https://510kreport.com/company/olympus-optical)
- Ethicon Endo-Surgery, Inc.: 4 (https://510kreport.com/company/ethicon-endo-surgery)
- Olympus Corp.: 2 (https://510kreport.com/company/olympus)
- Olympus America, Inc.: 1 (https://510kreport.com/company/olympus-america)
- Wilson-Cook Medical, Inc.: 1 (https://510kreport.com/company/wilson-cook-medical)
- Valleylab, Inc.: 1 (https://510kreport.com/company/valleylab)
- Mutoh America Co., Ltd.: 1 (https://510kreport.com/company/mutoh-america)

## Firms that cite its devices most
- Olympus Medical Systems Corp.: 5 (https://510kreport.com/company/olympus-medical-systems)

## Its most-cited devices
- K031523: Olympus Ultrasonic Surgical System (2003), cited by 4
- K031710: Olympus Ultrasonic Surgical System (2003), cited by 4
- K033333: Single Use 3-Lumen Balloon Catheter, Models B-230Q-a and B-230Q-B (2003), cited by 1

## Recent decisions
- K042160: Sonosurg Trocar (Jan 25, 2005)
- K041566: Sonosurg Ultrasonic Surgical System (Sep 8, 2004)
- K033333: Single Use 3-Lumen Balloon Catheter, Models B-230Q-a and B-230Q-B (Nov 14, 2003)
- K031523: Olympus Ultrasonic Surgical System (Oct 1, 2003)
- K031710: Olympus Ultrasonic Surgical System (Aug 29, 2003)
- K021672: Pancreatic Drainage Tube (Apr 16, 2003)
- K022446: Mucus Collection Probe, Models BC-401C & BC-402C (Mar 28, 2003)

Source page: https://510kreport.com/company/aomori-olympus