FDA applicant

Argus Biomedical Pty, Ltd.

Cincinnati, OH1 decision2002–20020 recalls

FDA records 1 decision for Argus Biomedical Pty, Ltd. (Cincinnati, OH) in 2002: 1 510(k) clearance. All are in product code HQM (Keratoprosthesis, Permanent Implant). 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, ophthalmic panel, where it files most

How often FDA has decided Argus Biomedical Pty, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Argus Biomedical Pty, Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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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 Cognitive, Inc. 3 Argus Photonics Group 2

Argus Biomedical Pty, Ltd.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Argus”