FDA applicant

Cimed Intl., Inc.

Mchenry, IL3 decisions1984–19840 recalls

FDA records 3 decisions for Cimed Intl., Inc. (Mchenry, IL) in 1984: 3 510(k) clearances. Most are in product codes HTD (Forceps) and DWP (Dilator, Vessel, Surgical). 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, general and plastic surgery panel, where it files most

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

FDA decisions per year

No FDA decision for Cimed Intl., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Cimed Intl., Inc.

Which product codes does it file in?

What has FDA decided for it lately?