FDA applicant

Lingeman Medical Products, Inc.

Indianapolis, IN1 decision1985–19850 recalls

FDA records 1 decision for Lingeman Medical Products, Inc. (Indianapolis, IN) in 1985: 1 510(k) clearance. All are in product code EYY (Drape, Urological, Disposable). 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 and plastic surgery panel, where it files most

How often FDA has decided Lingeman Medical Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Lingeman Medical Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Lingeman Medical Products, Inc.

Which product codes does it file in?

What has FDA decided for it lately?