510(k) Report

FDA applicant

Kinsei Shiatsu, Inc.

Torrance, CA6 decisions1995–19950 recalls

FDA records 6 decisions for Kinsei Shiatsu, Inc. (Torrance, CA) in 1995: 6 510(k) clearances. Most are in product codes ISA (Massager, Therapeutic, Electric) and IRO (Vibrator, Therapeutic). 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, physical medicine panel, where it files most

How often FDA has decided Kinsei Shiatsu, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Kinsei Shiatsu, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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

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