# Schneider Stent

- Location (FDA's records): Minneapolis, MN
- FDA decisions: 1 (1989–1989): 1 510(k) clearance
- Product codes: FGE (1)
- Predicates its devices cite: 0 (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 that cite its devices most
- Cordis Corp.: 2 (https://510kreport.com/company/cordis)

## Its most-cited devices
- K896163: Schneider Stent Wallstent Endoscopic Biliary Endo. (1989), cited by 2

## Recent decisions
- K896163: Schneider Stent Wallstent Endoscopic Biliary Endo. (Dec 1, 1989)

Source page: https://510kreport.com/company/schneider-stent