FDA applicant

Dupont Legal

Wilmington2 decisions1981–19830 recalls

FDA records 2 decisions for Dupont Legal (Wilmington) from 1981 to 1983: 2 original PMA approvals. Most are in product codes LPJ (Kit, Assay, Estrogen Receptor) and LPI (Kit, Assay, Progesterone Receptor). 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, clinical chemistry panel, where it files most

How often FDA has decided Dupont Legal’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Dupont Legal since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Dupont”

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

Dupont Medical Products 28 The Dupont Merck Pharmaceutical Co. 1

Dupont Legal

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Dupont”