FDA applicant

Monad Corp.

Pomona, CA9 decisions1989–19910 recalls

FDA records 9 decisions for Monad Corp. (Pomona, CA) from 1989 to 1991: 9 510(k) clearances. Most are in product codes GZJ (Stimulator, Nerve, Transcutaneous, For Pain…) and ISA (Massager, Therapeutic, Electric). 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, neurology panel, where it files most

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

FDA decisions per year

No FDA decision for Monad Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Monad Corp.

Which product codes does it file in?

What has FDA decided for it lately?