FDA applicant

Szabocsik and Assoc.

Chicago, IL4 decisions1994–19980 recalls

FDA records 4 decisions for Szabocsik and Assoc. (Chicago, IL) from 1994 to 1998: 4 510(k) clearances. Most are in product codes LPL (Lenses, Soft Contact, Daily Wear) and LPN (Accessories, Soft Lens Products). 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 Szabocsik and Assoc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Szabocsik and Assoc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Szabocsik”

FDA records each applicant name separately; these may or may not be the same firm.

Szabocsik and Associates 3

Szabocsik and Assoc.

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 “Szabocsik”