FDA applicant

Medie Group

Washington, DC1 decision1985–19850 recalls

FDA records 1 decision for Medie Group (Washington, DC) in 1985: 1 510(k) clearance. All are in product code KYP (Snake Bite Suction Kit). 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 hospital panel, where it files most

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

FDA decisions per year

No FDA decision for Medie Group since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Medie Group

Which product codes does it file in?

What has FDA decided for it lately?