FDA applicant

Microworld Medical Instruments, Inc.

Oakland, CA1 decision2003–20030 recalls

FDA records 1 decision for Microworld Medical Instruments, Inc. (Oakland, CA) in 2003: 1 510(k) clearance. All are in product code HQE (Instrument, Vitreous Aspiration And Cutting…). 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 Microworld Medical Instruments, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Microworld Medical Instruments, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Microworld Medical Instruments, Inc.

Which product codes does it file in?

What has FDA decided for it lately?