FDA applicant

Leonard P. Linkow, D.D.L.

Mchenry, IL1 decision1982–19820 recalls

FDA records 1 decision for Leonard P. Linkow, D.D.L. (Mchenry, IL) in 1982: 1 510(k) clearance. All are in product code NRQ (Blade-Form Endosseous Dental Implant). 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, dental panel, where it files most

How often FDA has decided Leonard P. Linkow, D.D.L.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Leonard P. Linkow, D.D.L. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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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 Joseph Co. 2 Leonard Lorch 1 Leonard Russo Co. 1

Leonard P. Linkow, D.D.L.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Leonard”