Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3009082125

FEI Number

3009082125

Entity Name

DAINIPPON SEIKI CO., LTD.

City/State/Country

Nagaokakyo Kyoto, JP

Establishment Address

Tanatsugu 8 Kotari, Nagaokakyo Kyoto 6170833, JP

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

DAINIPPON SEIKI CO., Ltd. (Owner Number: 10090054)

Owner / Operator Contact Address

Tanatsugu 8 Kotari, Nagaokakyo, JP-26 6170833, JP

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Auto Slide Preparation System FFPE Sample Block Automatic Facing Device

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KFL	Microtome, Sliding	Pathology	Class 1	864.3010	2024-02-07

Official Correspondent

Yoshiyuki Okumura

US Agent Details

Rhonda Alexander Business: IUVO Consulting, LLC Email: ralexander@iuvoconsulting.com Phone: (757) 5824337

Related Public Records

Same Entity

DAINIPPON SEIKI 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 3009082125. Last updated year: 2026. Please use registration number 3009082125 when referencing this establishment in official correspondence.