FDA applicant

Mansfield Scientific, Inc.

Mansfield, MA8 decisions1984–19870 recalls

FDA records 8 decisions for Mansfield Scientific, Inc. (Mansfield, MA) from 1984 to 1987: 8 510(k) clearances. Most are in product codes DTB (Permanent Pacemaker Electrode) and LDF (Electrode, Pacemaker, Temporary). 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 Mansfield Scientific, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Mansfield Scientific, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Mansfield Scientific, Inc.

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?