Kinsei Shiatsu, Inc.: FDA filings under this applicant name

FDA lists 6 510(k) clearances under the applicant name “Kinsei Shiatsu, Inc.” (first 1995, latest 1995), across 2 product codes in 1 review panel. Median 510(k) review time under this name: 41 days. Related companies, subsidiaries and acquired businesses that file under other applicant names are counted on their own pages, not here.

510(k) clearances per year

YearClearancesMedian review days
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Top product codes

Product codeDeviceSubmissions510(k) clearances
ISAMassager, Therapeutic, Electric55
IROVibrator, Therapeutic11

Review panels

Most recent Kinsei Shiatsu, Inc. 510(k) clearances

510(k)DeviceProduct codeDecision dateReview days
K952990SPIN ROLLEREISA1995-09-2993
K952916SHIATSU MASTER MASSAGER CUSHIONIRO1995-08-2863
K950411RELAXU-1ISA1995-08-02183
K950322RELAXY-THE WONDER HANDISA1995-02-1419
K950321SHAPE UP MOMI ROLLERISA1995-02-1419
K950320RELAXY-WONDER KNOCKISA1995-02-1419

Recalls

openFDA lists no recalls under a recalling firm named Kinsei Shiatsu, Inc..

Recalling firms are matched to this applicant name by name only (same normalization), so related entities that recall under another name are not counted. A recall count says nothing about how safe one company's devices are compared with another's.

Frequently asked questions

How many FDA 510(k) clearances are listed under Kinsei Shiatsu, Inc.?

FDA lists 6 510(k) clearances under the applicant name “Kinsei Shiatsu, Inc.” (first 1995, latest 1995), across 2 product codes in 1 review panel. Filings under other applicant names, such as subsidiaries, are not included.

How long has FDA taken to clear 510(k)s filed by Kinsei Shiatsu, Inc.?

The median time from FDA receipt to decision across 510(k)s cleared under the name Kinsei Shiatsu, Inc. is 41 days.

Which FDA product codes appear under Kinsei Shiatsu, Inc.?

The most frequent FDA product codes under this applicant name are ISA (Massager, Therapeutic, Electric, 5); IRO (Vibrator, Therapeutic, 1).

Next steps

Data from openFDA (510(k), PMA, De Novo, device recalls), ClinicalTrials.gov and SEC company tickers. Each page covers one FDA applicant name (spelling variants such as punctuation and legal suffixes combined); filings under other names are not included. Review days run from FDA receipt to decision. Not regulatory advice. Report an error in this data.

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