FDA applicant

Kamiya Tsusan Kaisha, Ltd.

Tokyo 100-91 Japan4 decisions1983–19860 recalls

FDA records 4 decisions for Kamiya Tsusan Kaisha, Ltd. (Tokyo 100-91 Japan) from 1983 to 1986: 4 510(k) clearances. Most are in product codes FWW (Table, Operating-Room, Pneumatic) and KQM (Camera, Surgical And Accessories). 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, general and plastic surgery panel, where it files most

How often FDA has decided Kamiya Tsusan Kaisha, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Kamiya Tsusan Kaisha, Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Kamiya Tsusan Kaisha, Ltd.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

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 Technology Services 2

Kamiya Tsusan Kaisha, Ltd.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Kamiya”