FDA applicant

Vista Lifesciences, Inc.

Parker, CO2 decisions2015–20210 recalls

FDA records 2 decisions for Vista Lifesciences, Inc. (Parker, CO) from 2015 to 2021: 2 510(k) clearances. Most are in product codes PKQ (Computerized Cognitive Assessment Aid) and POM (Computerized Cognitive Assessment Aid For…). Its devices cite 2 predicates, 0 of them its own earlier devices. 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 Vista Lifesciences, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2021

2015high 1 (2015) · low 0 (2016)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2015.

FIG. 1 — Vista Lifesciences, Inc. by year, 2015–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Vista Lifesciences, Inc.’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

Other applicant names beginning “Vista”

FDA records each applicant name separately; these may or may not be the same firm.

Vista Medical Technologies, Inc. 9 Vista Labs 2 Vista AI, Inc. 2 Vista Med 1 Vista Laboratories, Inc. 1 Vista Ophthalmics, LLC 1 Vista Products, Inc. 1 Vista Scientific, LLC 1 Vista Vision 1 Vista Medical Products, Inc. 1 Vista Industries,, LLC 1

Vista Lifesciences, Inc.

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?

Other applicant names beginning “Vista”