FDA applicant

Dimed, Intl.

Plant City, FL3 decisions1986–19870 recalls

FDA records 3 decisions for Dimed, Intl. (Plant City, FL) from 1986 to 1987: 3 510(k) clearances. Most are in product codes KKX (Drape, Surgical, Antimicrobial) and JSH (Culture Media, Non-Selective And Differential). 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 Dimed, Intl.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Dimed, Intl. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Dimed, Intl.

Which product codes does it file in?

What has FDA decided for it lately?