Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3025032529

FEI Number

3025032529

Entity Name

VIVATEC CO.,LTD.

City/State/Country

Sakai-shi Osaka, JP

Establishment Address

2-10-1,Kitahanada-cho,Kita-ku,, Sakai-shi Osaka 591-8002, JP

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer),Manufacture Medical Device

Owner / Operator

VIVATEC Co.,Ltd. (Owner Number: 10092839)

Owner / Operator Contact Address

2-10-1,Kitahanada-cho,Kita-ku,, Sakai-shi, JP-27 591-8002, JP

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

TOOTHBRUSH, MANUAL

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
EFW	Toothbrush, Manual	Dental	Class 1	872.6855	2025-02-25

Official Correspondent

Yoshio Matsumoto

US Agent Details

Dean-Paul Hart Business: Frederick Hart Co., Inc. Email: compliance@compacind.com Phone: (404) 3734030

Related Public Records

Same Entity

VIVATEC Co.,Ltd.

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

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K973236	Procter & Gamble Co.	CREST TOOTHBRUSH WITH MICROSHIELD	1998-03-11

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3025032529. Last updated year: 2026. Please use registration number 3025032529 when referencing this establishment in official correspondence.