# Schneider Intl., Ltd.

- Location (FDA's records): Plymouth, MN
- FDA decisions: 22 (1989–1995): 22 510(k) clearances
- Product codes: LIT (8), DQO (4), DQX (4), DQY (3), FGE (2), DXY (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 9 (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)
- Boston Scientific Corp: 2 (https://510kreport.com/company/boston-scientific)
- Boston Scientific Scimed, Inc.: 2 (https://510kreport.com/company/boston-scientific-scimed)
- Lumend, Inc.: 1 (https://510kreport.com/company/lumend)
- Bridgepoint Medical: 1 (https://510kreport.com/company/bridgepoint-medical)
- Medinol, Ltd.: 1 (https://510kreport.com/company/medinol)

## Its most-cited devices
- K925406: Biliary Endoprostheses W/Unistep Delivery System (1995), cited by 3
- K885180: Expandable Biliary Stent Endoprosthesis (1989), cited by 2
- K911547: Magnum-Meier Recanalization Guidewire (1991), cited by 2
- K926271: Schneider Match-35 Percutaneous Transluminal Angio (1993), cited by 1
- K913297: Schneider Match-35(TM) Percu Trans Angioplas Cath (1991), cited by 1

## Recent decisions
- K925406: Biliary Endoprostheses W/Unistep Delivery System (Jan 11, 1995)
- K931577: Schneider Magnum Peripheral Recanalization Guidewi (Jun 23, 1993)
- K926271: Schneider Match-35 Percutaneous Transluminal Angio (Jun 7, 1993)
- K926003: Schneider Softip SST Angiographic (Diag) Catheter (Jun 7, 1993)
- K925804: Schneider Hydro-Sil Guidewire (Feb 12, 1993)
- K924591: Schneider Solid-7 Soptip Guiding Catheter (Dec 8, 1992)
- K921856: Total Cross .021 Percut. Transluminal Angio. Cath. (Jul 21, 1992)
- K921943: Schneider Monorail 421 Percu Trans Angio (Pta) Bal (Jun 17, 1992)

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