FDA applicant

Digital Applications, Inc.

Santaquin, UT1 decision1997–19970 recalls

FDA records 1 decision for Digital Applications, Inc. (Santaquin, UT) in 1997: 1 510(k) clearance. All are in product code KPN (Alarm, Conditioned Response Enuresis). 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, gastroenterology and urology panel, where it files most

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

FDA decisions per year

No FDA decision for Digital Applications, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Digital Applications, Inc.

Which product codes does it file in?

What has FDA decided for it lately?