FDA applicant

Kamiya Technology Services

Westport, CT2 decisions1996–19960 recalls

FDA records 2 decisions for Kamiya Technology Services (Westport, CT) in 1996: 2 510(k) clearances. All are in product code DHR (System, Test, Rheumatoid Factor). 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, immunology panel, where it files most

How often FDA has decided Kamiya Technology Services’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Kamiya Technology Services since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Kamiya”

FDA records each applicant name separately; these may or may not be the same firm.

Kamiya Biomedical Co. 46 Kamiya Tsusan Kaisha, Ltd. 4

Kamiya Technology Services

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?

Other applicant names beginning “Kamiya”