FDA applicant

Cane S.R.L.

Deer Field, IL10 decisions2001–20091 recall

FDA records 10 decisions for Cane S.R.L. (Deer Field, IL) from 2001 to 2009: 10 510(k) clearances. Most are in product codes FRN (Pump, Infusion) and MEA (Pump, Infusion, Pca). Its devices cite 12 predicates, 7 of them its own earlier devices. 1 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, general hospital panel, where it files most

How often FDA has decided Cane S.R.L.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2009

2007high 1 (2009) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

1in 2013

2007high 1 (2013) · low 0 (2007)2026

Class I Class II/III not classified

FIG. 1 — Cane S.R.L. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Cane S.R.L.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Other applicant names beginning “Cane”

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

Cane S.R.I. 2

Cane S.R.L.

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

What has been recalled?

Other applicant names beginning “Cane”