FDA applicant

Inter Med Industries, Inc.

Mchenry, IL3 decisions1980–19810 recalls

FDA records 3 decisions for Inter Med Industries, Inc. (Mchenry, IL) from 1980 to 1981: 3 510(k) clearances. Most are in product codes GZJ (Stimulator, Nerve, Transcutaneous, For Pain…) and IPF (Stimulator, Muscle, 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, neurology panel, where it files most

How often FDA has decided Inter Med Industries, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Inter Med Industries, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Inter Med Industries, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Other applicant names beginning “Inter”

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

Inter-Med, Inc. 12 Inter-Med/Vista Dental Products 6 Inter Medical Medizintechnik GmbH 3 Inter Science Institute 3 Inter-Os Technologies 2 Inter Continental Health Care 2 Inter-Asia Co., Inc. 1 Inter-Pal GmbH 1 Inter-Med / Vista Dental 1 Inter-Continental Industries Sdn Bhd 1

Inter Med Industries, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Inter”