FDA applicant

Seare Biomedical Corp.

Salt Lake City, UT8 decisions1998–19980 recalls

FDA records 8 decisions for Seare Biomedical Corp. (Salt Lake City, UT) in 1998: 8 510(k) clearances. Most are in product codes MIB (Elastomer, Silicone Block) and MIC (Implant, Muscle, Pectoralis). 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, ear, nose and throat panel, where it files most

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

FDA decisions per year

No FDA decision for Seare Biomedical Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Seare Biomedical 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?