FDA applicant

Continental Optical Imports

Chicago, IL2 decisions1994–19940 recalls

FDA records 2 decisions for Continental Optical Imports (Chicago, IL) in 1994: 2 510(k) clearances. All are in product code HQZ (Frame, Spectacle). 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 Continental Optical Imports’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Continental Optical Imports since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Continental”

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

Continental X-Ray Corp. 27 Continental Medical Laboratories, Inc. 8 Continental Soft Lens, Inc. 2 Continental Dental Laboratory 1 Continental Dental Ceramics, Inc. (Dba Continental 1 Continental Scale Corp. 1 Continental Dental Ceramics, Inc. 1 Continental Products, Inc. 1

Continental Optical Imports

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Continental”