FDA applicant

Inmed Corp.

Mchenry, IL35 decisions1981–20031 recall

FDA records 35 decisions for Inmed Corp. (Mchenry, IL) from 1981 to 2003: 35 510(k) clearances. Most are in product codes KNT (Tubes, Gastrointestinal (And Accessories)) and KOD (Catheter, Urological). Its devices cite 3 predicates, 0 of them its own earlier devices. 1 recall is linked to its devices.

FDA’s records also spell it “Inmed Ltda.”.

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 Inmed Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Inmed Corp. since 2007.

Recalls per year

1in 2018

2007high 1 (2018) · low 0 (2007)2026

Class I Class II/III not classified

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

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

See the 510(k) Report

Other applicant names beginning “Inmed”

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

Inmed Gloves Factory 1

Inmed Corp.

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

What has been recalled?

Other applicant names beginning “Inmed”