FDA applicant

Numotech, Inc.

Sun Valley, CA2 decisions1995–19990 recalls

FDA records 2 decisions for Numotech, Inc. (Sun Valley, CA) from 1995 to 1999: 2 510(k) clearances. Most are in product codes IOQ (Bed, Flotation Therapy, Powered) and KPJ (Chamber, Oxygen, Topical, Extremity). 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, physical medicine panel, where it files most

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

FDA decisions per year

No FDA decision for Numotech, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Numotech, Inc.

Which product codes does it file in?

What has FDA decided for it lately?