FDA applicant

Micro Specialties, Inc.

Milford, CT4 decisions1998–20040 recalls

FDA records 4 decisions for Micro Specialties, Inc. (Milford, CT) from 1998 to 2004: 4 510(k) clearances. All are in product code HNO (Keratome, Ac-Powered). Its devices cite 5 predicates, 0 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, ophthalmic panel, where it files most

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

FDA decisions per year

No FDA decision for Micro Specialties, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Micro Specialties, 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?