FDA applicant

Deip Enterprises, Inc.

Mchenry, IL4 decisions1983–19830 recalls

FDA records 4 decisions for Deip Enterprises, Inc. (Mchenry, IL) in 1983: 4 510(k) clearances. All are in product code IQK (Orthosis, Cervical). 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, physical medicine panel, where it files most

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

FDA decisions per year

No FDA decision for Deip Enterprises, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Deip Enterprises, Inc.

Which product codes does it file in?

What has FDA decided for it lately?