FDA applicant

Becton Dickinson Inc. (Bd)

Salt Lake Ciy,, UT1 decision2025–20250 recalls

FDA records 1 decision for Becton Dickinson Inc. (Bd) (Salt Lake Ciy,, UT) in 2025: 1 510(k) clearance. All are in product code SEF (Central Venous Catheter With Manual Insertion…). Its devices cite 1 predicate, 0 of them its own earlier devices. 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, general hospital panel, where it files most

How often FDA has decided Becton Dickinson Inc. (Bd)’s devices, and how often a recall has named them.

FDA decisions per year

1in 2025

2025high 1 (2025)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2025.

FIG. 1 — Becton Dickinson Inc. (Bd) by year, 2025–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Becton”

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

Becton, Dickinson & CO 342 Becton Dickinson Infusion Therapy Systems, Inc. 36 Becton Dickinson Microbiology Systems 33 Becton Dickinson Vascular Access, Inc. 25 Becton Dickinson Immunocytometry Systems 21 Becton Dickinson Vacutainer Systems 15 Becton Dickinson Diagnostic Instrument Systems 13 Becton Dickinson Advanced Diagnostics 10 Becton, Dickinson and Company (BD) 5 Becton Dickinson Labware 3 Becton Dickinson Consumer Products 3 Becton Dickinson Biosciences 1

Becton Dickinson Inc. (Bd)

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “Becton”