# Schneider U.S. Stent Div.

- Location (FDA's records): Plymouth, MN
- FDA decisions: 3 (1991–1994): 3 510(k) clearances
- Product codes: FGE (2), ESW (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 10 (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
- Boston Scientific Scimed, Inc.: 6 (https://510kreport.com/company/boston-scientific-scimed)
- Cordis Corp.: 3 (https://510kreport.com/company/cordis)
- Schneider (Europe) GmbH: 1 (https://510kreport.com/company/schneider-europe)

## Its most-cited devices
- K923993: Wallstent Biliary Endoprotheses (1994), cited by 4
- K914277: Wallstent (R) Trans Biliary Endo W/Unistep Deliv SY (1991), cited by 4
- K923119: Wallstent Esophageal Prothesis (1992), cited by 2

## Recent decisions
- K923993: Wallstent Biliary Endoprotheses (Sep 30, 1994)
- K923119: Wallstent Esophageal Prothesis (Sep 1, 1992)
- K914277: Wallstent (R) Trans Biliary Endo W/Unistep Deliv SY (Nov 29, 1991)

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