FDA applicant

Argus Medical Co., Inc.

Walnut, CA6 decisions1995–19950 recalls

FDA records 6 decisions for Argus Medical Co., Inc. (Walnut, CA) in 1995: 6 510(k) clearances. Most are in product codes HRX (Arthroscope) and GCJ (Laparoscope, General & Plastic Surgery). 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, orthopedic panel, where it files most

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

FDA decisions per year

No FDA decision for Argus Medical Co., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Argus Medical Co., 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 Cognitive, Inc. 3 Argus Photonics Group 2 Argus Biomedical Pty, Ltd. 1

Argus Medical Co., Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Argus”