510(k) Report

FDA applicant

E Med Future

Millersburg1 decision2003–20030 recalls

FDA records 1 decision for E Med Future (Millersburg) in 2003: 1 original PMA approval. All are in product code MTV (Sharps Needle Destruction Device). 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 E Med Future’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for E Med Future since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Which product codes does it file in?

  • MTVSharps Needle Destruction Device1decision

What has FDA decided for it lately?

  • P010065Needle Zap (R)E Med Future · 2003

The one decision as E Med Future →