FDA applicant

Expertech Assoc., Inc.

Concord, MA2 decisions1995–19960 recalls

FDA records 2 decisions for Expertech Assoc., Inc. (Concord, MA) from 1995 to 1996: 2 510(k) clearances. Most are in product codes HJO (Biomicroscope, Slit-Lamp, Ac-Powered) and HLQ (Keratoscope, Ac-Powered). 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 Expertech Assoc., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Expertech Assoc., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Expertech Assoc., Inc.

Which product codes does it file in?

What has FDA decided for it lately?