# Schneider (Europe) GmbH

- Location (FDA's records): Bulach, SE
- FDA decisions: 5 (1995–1999): 5 510(k) clearances
- Product codes: DQX (4), ESW (1)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 1 (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 whose devices it cites most
- Boston Scientific Scimed, Inc.: 1 (https://510kreport.com/company/boston-scientific-scimed)
- Schneider U.S. Stent Div.: 1 (https://510kreport.com/company/schneider-us-stent-div)

## Firms that cite its devices most
- Lumend, Inc.: 1 (https://510kreport.com/company/lumend)

## Its most-cited devices
- K970528: Clyde Coronary Guidewire (1997), cited by 1

## Recent decisions
- K984068: Flamingo Wallstent Esophageal Endoprosthesis (Jan 7, 1999)
- K982592: Docking-Extension Wire (Oct 21, 1998)
- K970528: Clyde Coronary Guidewire (Jun 10, 1997)
- K970494: Hannibal Guidewire (May 9, 1997)
- K951109: C-Thru Coronary Guide Wire (Jun 8, 1995)

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