FDA applicant

Landmark Plastics

Mchenry, IL13 decisions1976–19760 recalls

FDA records 13 decisions for Landmark Plastics (Mchenry, IL) in 1976: 13 510(k) clearances. Most are in product codes FNY (Basin, Emesis) and FOB (Bedpan). 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 Landmark Plastics’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Landmark Plastics since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Landmark Plastics’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 “Landmark”

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

Landmark Scientific, Inc. 1

Landmark Plastics

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Landmark”