FDA applicant

Unipower Corp.

Minneapolis, MN3 decisions1994–19940 recalls

FDA records 3 decisions for Unipower Corp. (Minneapolis, MN) in 1994: 3 510(k) clearances. Most are in product codes LDD (Dc-Defibrillator, Low-Energy, (Including…) and BXP (Transducer, Gas Flow). 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, cardiovascular panel, where it files most

How often FDA has decided Unipower Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Unipower Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Unipower Corp.

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?