FDA applicant

Keisei (Usa) Co., Ltd.

Torrance, CA2 decisions1993–19960 recalls

FDA records 2 decisions for Keisei (Usa) Co., Ltd. (Torrance, CA) from 1993 to 1996: 2 510(k) clearances. Most are in product codes FNM (Mattress, Air Flotation, Alternating Pressure) and CAE (Airway, Oropharyngeal, Anesthesiology). 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 hospital panel, where it files most

How often FDA has decided Keisei (Usa) Co., Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Keisei (Usa) Co., Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Keisei (Usa) Co., Ltd. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Keisei (Usa) Co., 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 “Keisei”

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

Keisei Medical Industrial Co., Ltd. 4

Keisei (Usa) Co., Ltd.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Keisei”