FDA applicant

Meridian Medical

Irvine, CA1 decision2006–20060 recalls

FDA records 1 decision for Meridian Medical (Irvine, CA) in 2006: 1 510(k) clearance. All are in product code LXT (Appliance, Fixation, Nail/Blade/Plate…). Its devices cite 1 predicate, 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, orthopedic panel, where it files most

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

FDA decisions per year

No FDA decision for Meridian Medical since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Meridian”

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

Meridian Diagnostics, Inc. 92 Meridian Bioscience, Inc. 39 Meridian AG 14 Meridian Medical Systems, LLC 8 Meridian Medical Technologies, Inc. 6 Meridian Bioscience Israel, Ltd. 3 Meridian Technique, Ltd. 1 Meridian Dynamics Biomedical, Inc. 1

Meridian Medical

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “Meridian”