FDA applicant

Maxxvision, LLC

Gainesville, FL1 decision2003–20030 recalls

FDA records 1 decision for Maxxvision, LLC (Gainesville, FL) 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 Maxxvision, LLC’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Maxxvision, LLC since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Maxxvision, LLC’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Maxxvision, LLC

Which product codes does it file in?

What has FDA decided for it lately?