510(k) Report

FDA applicant

Vocel

Washington, DC1 decision2006–20060 recalls

FDA records 1 decision for Vocel (Washington, DC) in 2006: 1 510(k) clearance. All are in product code NXQ (Reminder, Medication). 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, physical medicine panel, where it files most

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

FDA decisions per year

No FDA decision for Vocel since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Vocel 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?

  • NXQReminder, Medication1decision

Who builds on its devices?

Later devices cite its devices 1 time; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K060298Pill PhoneVocel · 20061cites it

What has FDA decided for it lately?

The one decision as Vocel →