FDA applicant

Design Med. Corp.

Lake Forest, IL3 decisions1984–19850 recalls

FDA records 3 decisions for Design Med. Corp. (Lake Forest, IL) from 1984 to 1985: 3 510(k) clearances. All are in product code HLJ (Ophthalmoscope, Battery-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 Design Med. Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Design Med. Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Design”

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

Design Technologies, Inc. 4 Design Research Assoc., Inc. 3 Design Standards Corp. 2 Design Principles, Inc. 1 Design Specific Fletcher 1 Design & Manufacturing Consultants 1 Design Specific, Ltd. 1

Design Med. Corp.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Design”