# Koninklijke Utermohlen NV

- Location (FDA's records): San Diego, CA
- FDA decisions: 2 (2011–2013): 2 510(k) clearances
- Product codes: GEH (2)
- Predicates its devices cite: 3 (1 its own); citations of its devices by later devices: 3 (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
- Wartner Medical Products: 1 (https://510kreport.com/company/wartner-medical-products)
- OraSure Technologies, Inc.: 1 (https://510kreport.com/company/orasure-technologies)

## Firms that cite its devices most
- Pronova Laboratories BV: 1 (https://510kreport.com/company/pronova-laboratories)
- Yonmedical BV: 1 (https://510kreport.com/company/yonmedical)

## Its most-cited devices
- K130599: Wart Freeze (2013), cited by 2
- K101049: Wart Freeze (2011), cited by 1

## Recent decisions
- K130599: Wart Freeze (Jun 5, 2013)
- K101049: Wart Freeze (Jun 23, 2011)

Source page: https://510kreport.com/company/koninklijke-utermohlen