FDA applicant

Solution Technologies

South Ogden, UT2 decisions1998–19981 recall

FDA records 2 decisions for Solution Technologies (South Ogden, UT) in 1998: 2 510(k) clearances. All are in product code KPO (Dialysate Concentrate For Hemodialysis (Liquid…). 1 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 Solution Technologies’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Solution Technologies since 2007.

Recalls per year

1in 2012

2007high 1 (2012) · low 0 (2007)2026

Class I Class II/III not classified

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

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Solution Technologies

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

What has been recalled?