FDA applicant

Solohill Engineering, Inc.

Ann Arbor, MI1 decision1985–19850 recalls

FDA records 1 decision for Solohill Engineering, Inc. (Ann Arbor, MI) in 1985: 1 510(k) clearance. All are in product code KJB (Apparatus, Roller). 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, hematology panel, where it files most

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

FDA decisions per year

No FDA decision for Solohill Engineering, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Solohill Engineering, Inc.

Which product codes does it file in?

What has FDA decided for it lately?