FDA applicant
Kinsei Shiatsu, Inc.
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
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.
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.
See the 510(k) Report