FDA applicant

Foley & Lardner

Washington, DC5 decisions1994–19980 recalls

FDA records 5 decisions for Foley & Lardner (Washington, DC) from 1994 to 1998: 5 510(k) clearances. Most are in product codes KNN (Components, Wheelchair) and DXN (System, Measurement, Blood-Pressure…). 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, physical medicine panel, where it files most

How often FDA has decided Foley & Lardner’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Foley & Lardner since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Foley”

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

Foley, Lardner, Hollabaugh & Jacobs 1

Foley & Lardner

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Foley”