FDA applicant

Smartpractice

Phoenix, AZ4 decisions2002–20120 recalls

FDA records 4 decisions for Smartpractice (Phoenix, AZ) from 2002 to 2012: 4 510(k) clearances. Most are in product codes KXF (Applicator, Absorbent Tipped, Non-Sterile) and EFS (Unit, Oral Irrigation). 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 Smartpractice’s devices, and how often a recall has named them.

FDA decisions per year

1in 2012

2007high 1 (2011) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

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Smartpractice

Which product codes does it file in?

What has FDA decided for it lately?