FDA applicant

International Medical Devices, Inc.

Beverly Hills, CA4 decisions2017–20230 recalls

FDA records 4 decisions for International Medical Devices, Inc. (Beverly Hills, CA) from 2017 to 2023: 4 510(k) clearances. All are in product code MIB (Elastomer, Silicone Block). Its devices cite 10 predicates, 5 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, ear, nose and throat panel, where it files most

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

FDA decisions per year

1in 2023

2017high 1 (2017) · low 0 (2018)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2017.

FIG. 1 — International Medical Devices, Inc. by year, 2017–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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International Medical Devices, 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?