FDA applicant

Landmark Scientific, Inc.

Rockville, MD1 decision1997–19970 recalls

FDA records 1 decision for Landmark Scientific, Inc. (Rockville, MD) in 1997: 1 510(k) clearance. All are in product code JJG (Analyzer, Chemistry, Centrifugal, For Clinical…). Its devices cite 2 predicates, 0 of them its own earlier devices. 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, clinical chemistry panel, where it files most

How often FDA has decided Landmark Scientific, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Landmark Scientific, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Landmark Scientific, Inc.’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 Plastics 13

Landmark Scientific, Inc.

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “Landmark”