# Zutron Medical, LLC

- Location (FDA's records): Lenexa, KS
- FDA decisions: 2 (2005–2010): 2 510(k) clearances
- Names in FDA's records: Zutron Medical, LLC (1); Zutron Medical (1)
- Product codes: FCY (1), FDF (1)
- Predicates its devices cite: 4 (0 its own); citations of its devices by later devices: 2 (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
- Wilson-Cook Medical, Inc.: 1 (https://510kreport.com/company/wilson-cook-medical)
- Medi-Globe Corp.: 1 (https://510kreport.com/company/medi-globe)
- Endo-Therapeutics, Inc.: 1 (https://510kreport.com/company/endo-therapeutics)
- Olympus Optical Co., Ltd.: 1 (https://510kreport.com/company/olympus-optical)

## Firms that cite its devices most
- FUJIFILM Healthcare Americas Corporation: 1 (https://510kreport.com/company/fujifilm-healthcare-americas)
- Olympus Medical Systems Corp.: 1 (https://510kreport.com/company/olympus-medical-systems)

## Its most-cited devices
- K093718: Zutron Medical Endoscope Leak Tester Model Zutr-10003 (2010), cited by 1
- K051068: Zutron Colonoscope Stiffening Device (2005), cited by 1

## Recent decisions
- K093718: Zutron Medical Endoscope Leak Tester Model Zutr-10003 (Feb 22, 2010)
- K051068: Zutron Colonoscope Stiffening Device (Jul 11, 2005)

Source page: https://510kreport.com/company/zutron-medical