# Wartner Medical Products

- Location (FDA's records): Brampton, Ontario, CA
- FDA decisions: 3 (2000–2003): 3 510(k) clearances
- Product codes: GEH (3)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 4 (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 that cite its devices most
- OraSure Technologies, Inc.: 2 (https://510kreport.com/company/orasure-technologies)
- Schering-Plough Healthcare Products, Inc.: 1 (https://510kreport.com/company/schering-plough-healthcare-products)
- Koninklijke Utermohlen NV: 1 (https://510kreport.com/company/koninklijke-utermohlen)

## Its most-cited devices
- K011708: Modification to Wartner Wart Removal System (2002), cited by 4

## Recent decisions
- K030838: Wartner Pro (Jun 27, 2003)
- K011708: Modification to Wartner Wart Removal System (Feb 20, 2002)
- K002714: Wartner Wart Removal System (Nov 28, 2000)

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