FDA applicant

Poretics Corp.

Livermore, CA1 decision1987–19870 recalls

FDA records 1 decision for Poretics Corp. (Livermore, CA) in 1987: 1 510(k) clearance. All are in product code KET (Filters, Cell Collection, Tissue Processing). 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, pathology panel, where it files most

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

FDA decisions per year

No FDA decision for Poretics Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Poretics Corp.

Which product codes does it file in?

What has FDA decided for it lately?