FDA applicant

Argus Cognitive, Inc.

Hanover, NH3 decisions2023–20260 recalls

FDA records 3 decisions for Argus Cognitive, Inc. (Hanover, NH) from 2023 to 2026: 3 510(k) clearances. Most are in product codes LLZ (System, Image Processing, Radiological) and QIH (Automated Radiological Image Processing Software). Its devices cite 3 predicates, 1 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, radiology panel, where it files most

How often FDA has decided Argus Cognitive, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2023

2023high 2 (2026) · low 0 (2024)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2023.

FIG. 1 — Argus Cognitive, Inc. by year, 2023–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Argus Cognitive, 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 “Argus”

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

Argus Medical Co., Inc. 6 Argus Photonics Group 2 Argus Biomedical Pty, Ltd. 1

Argus Cognitive, Inc.

Which product codes does it file in?

Whose devices does it build on?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Argus”