FDA applicant

Senticare, Inc.

Washington, DC1 decision2011–20110 recalls

FDA records 1 decision for Senticare, Inc. (Washington, DC) in 2011: 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 Senticare, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2011

2011high 1 (2011) · low 0 (2012)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2011.

FIG. 1 — Senticare, Inc. by year, 2011–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Senticare, Inc.

Which product codes does it file in?

What has FDA decided for it lately?