FDA applicant

Medical Electronic Assn.

Englewood, CO3 decisions1986–19910 recalls

FDA records 3 decisions for Medical Electronic Assn. (Englewood, CO) from 1986 to 1991: 3 510(k) clearances. Most are in product codes GZJ (Stimulator, Nerve, Transcutaneous, For Pain…) and GXY (Electrode, Cutaneous). 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 Medical Electronic Assn.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Medical Electronic Assn. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Medical Electronic Assn.

Which product codes does it file in?

What has FDA decided for it lately?