FDA applicant

Numa, Inc.

Amherst, NH3 decisions1993–20000 recalls

FDA records 3 decisions for Numa, Inc. (Amherst, NH) from 1993 to 2000: 3 510(k) clearances. Most are in product codes LLZ (System, Image Processing, Radiological) and KPS (System, Tomography, Computed, Emission). Its devices cite 1 predicate, 0 of them its own earlier devices. No recall is linked to its devices.

FDA’s records also spell it “Numa Corp.”.

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 Numa, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Numa, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Numa, Inc.

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?