# Escalon Trek Medical

- Location (FDA's records): Mukwonago, WI
- FDA decisions: 3 (1992–1996): 3 510(k) clearances
- Product codes: KYG (1), MPA (1), MRH (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: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Dutch Ophthalmic USA, Inc.: 2 (https://510kreport.com/company/dutch-ophthalmic-usa)
- Storz Instrument Co.: 1 (https://510kreport.com/company/storz-instrument)
- Vision Pro, LLC: 1 (https://510kreport.com/company/vision-pro)
- Iscience Surgical Corporation: 1 (https://510kreport.com/company/iscience-surgical)

## Its most-cited devices
- K963434: Viscous Fluid System (1996), cited by 3
- K963417: Vitlite (TR7700) (1996), cited by 2

## Recent decisions
- K963417: Vitlite (TR7700) (Dec 20, 1996)
- K963434: Viscous Fluid System (Nov 25, 1996)
- K924999: Autopole Regulator System (Dec 24, 1992)

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