510(k) Report

FDA applicant

Connexmd

Seattle, WA1 decision2003–20030 recalls

FDA records 1 decision for Connexmd (Seattle, WA) in 2003: 1 510(k) clearance. All are in product code LLZ (System, Image Processing, Radiological). 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 Connexmd’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Connexmd since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Which product codes does it file in?

  • LLZSystem, Image Processing, Radiological1decision

What has FDA decided for it lately?

  • K033093Echoconnex CommunicatorConnexmd · 2003

The one decision as Connexmd →