FDA applicant

Leonard Joseph Co.

Walker, MI2 decisions1983–19850 recalls

FDA records 2 decisions for Leonard Joseph Co. (Walker, MI) from 1983 to 1985: 2 510(k) clearances. Most are in product codes KGX (Tape And Bandage, Adhesive) and EFQ (Gauze/Sponge, Internal). 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 Leonard Joseph Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Leonard Joseph Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Leonard Joseph 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 “Leonard”

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

Leonard Medical, Inc. 7 Leonard Lorch 1 Leonard P. Linkow, D.D.L. 1 Leonard Russo Co. 1

Leonard Joseph Co.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Leonard”