FDA applicant

Becton Dickson & Co.

Franklin Lakes, NJ1 decision2009–20090 recalls

FDA records 1 decision for Becton Dickson & Co. (Franklin Lakes, NJ) in 2009: 1 510(k) clearance. All are in product code BSP (Needle, Conduction, Anesthetic (W/Wo Introducer)). 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, anesthesiology panel, where it files most

How often FDA has decided Becton Dickson & Co.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2009

2009high 1 (2009) · low 0 (2010)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2009.

FIG. 1 — Becton Dickson & Co. by year, 2009–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Becton Dickson & Co.’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 “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 Dickson & Co.

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 “Becton”