FDA applicant

Septa Corp.

Mason, NH1 decision1995–19950 recalls

FDA records 1 decision for Septa Corp. (Mason, NH) in 1995: 1 510(k) clearance. All are in product code KXJ (Table, Radiologic). 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, radiology panel, where it files most

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

FDA decisions per year

No FDA decision for Septa Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Septa Corp.

Which product codes does it file in?

What has FDA decided for it lately?