FDA applicant

Intermed, Inc.

Mchenry, IL16 decisions1976–19900 recalls

FDA records 16 decisions for Intermed, Inc. (Mchenry, IL) from 1976 to 1990: 16 510(k) clearances. Most are in product codes KNX (Collector, Urine, (And Accessories) For…) and KOD (Catheter, Urological). 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, gastroenterology and urology panel, where it files most

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

FDA decisions per year

No FDA decision for Intermed, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Intermed”

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

Intermed Group, Inc. 1 Intermed Advisors, Inc. 1

Intermed, Inc.

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 “Intermed”