Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3011504786

FEI Number

3011504786

Entity Name

SANYOSEIKO CO., LTD.

City/State/Country

Otsuki-shi Yamanashi, JP

Establishment Address

1150, Shimowada, Nanaho-machi, Otsuki-shi Yamanashi 409-0622, JP

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

SANYOSEIKO CO., LTD. (Owner Number: 10054424)

Owner / Operator Contact Address

1435, Ozawa, Saruhashi-machi, Otsuki-shi, JP-19 409-0616, JP

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K072882

PMA Number

N/A

All Registered Proprietary Names

PS-2100

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
LLN	Device, Vibration Threshold Measurement	Neurology	Class 1	882.1200	2018-12-21

Official Correspondent

FUTOSHI SHIRAKAWA

US Agent Details

Kenneth Block Email: k.block@kenblockconsulting.com Phone: (972) 4809554

Related Public Records

Same Entity

SANYOSEIKO CO., LTD.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3011504786. Last updated year: 2026. Please use registration number 3011504786 when referencing this establishment in official correspondence.