FDA applicant

Usci, Div. C.R. Bard, Inc.

Mchenry, IL13 decisions1976–19950 recalls

FDA records 13 decisions for Usci, Div. C.R. Bard, Inc. (Mchenry, IL) from 1976 to 1995: 12 510(k) clearances and 1 original PMA approval. Most are in product codes DSY (Prosthesis, Vascular Graft, Of 6mm And Greater…) and DYB (Introducer, Catheter). 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 Usci, Div. C.R. Bard, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Usci, Div. C.R. Bard, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Usci, Div. C.R. Bard, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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

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Other applicant names beginning “Usci”

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

Usci Ireland 2

Usci, Div. C.R. Bard, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Usci”