FDA applicant

Keta Corp.

Danvers, MA3 decisions1984–19860 recalls

FDA records 3 decisions for Keta Corp. (Danvers, MA) from 1984 to 1986: 3 510(k) clearances. Most are in product codes HPT (Perimeter, Automatic, Ac-Powered) and HKS (Prism, Gonioscopic). 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, ophthalmic panel, where it files most

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

FDA decisions per year

No FDA decision for Keta Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Keta Corp.

Which product codes does it file in?

What has FDA decided for it lately?