FDA applicant

Mimvista Corp.

Cleveland, OH4 decisions2005–20072 recalls

FDA records 4 decisions for Mimvista Corp. (Cleveland, OH) from 2005 to 2007: 4 510(k) clearances. All are in product code LLZ (System, Image Processing, Radiological). Its devices cite 13 predicates, 3 of them its own earlier devices. 2 recalls are 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 Mimvista Corp.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2007

2007high 1 (2007) · low 0 (2008)2026

2026 so far, outlined.

Recalls per year

1in 2025

2007high 1 (2008) · low 0 (2007)2026

Class I Class II/III not classified

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

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Mimvista Corp.

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

What has been recalled?