FDA applicant

Meyra, Inc.

Matthews, NC3 decisions2005–20050 recalls

FDA records 3 decisions for Meyra, Inc. (Matthews, NC) in 2005: 3 510(k) clearances. All are in product code IOR (Wheelchair, Mechanical). No recall is linked to its devices.

FDA’s records also spell it “Meyra”.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, physical medicine panel, where it files most

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

FDA decisions per year

No FDA decision for Meyra, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Meyra, Inc.

Which product codes does it file in?

What has FDA decided for it lately?