FDA applicant

Schneider-Shilley (Usa)

Minneapolis, MN9 decisions1988–19890 recalls

FDA records 9 decisions for Schneider-Shilley (Usa) (Minneapolis, MN) from 1988 to 1989: 9 510(k) clearances. Most are in product codes LIT (Catheter, Angioplasty, Peripheral, Transluminal) and DQO (Catheter, Intravascular, Diagnostic). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, cardiovascular panel, where it files most

How often FDA has decided Schneider-Shilley (Usa)’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Schneider-Shilley (Usa) since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Schneider-Shilley (Usa) by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Schneider-Shilley”

FDA records each applicant name separately; these may or may not be the same firm.

Schneider Intl., Ltd. 22 Schneider (Europe) GmbH 5 Schneider U.S. Stent Div. 3 Schneider/Namic 2 Schneider Stent 1

Schneider-Shilley (Usa)

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Schneider-Shilley”