Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3005674561

FEI Number

3005674561

Entity Name

LIVEDO CORPORATION

City/State/Country

CHUO KU OSAKA, JP

Establishment Address

Yodoyabashi Center Bldg. 8F-9F, 3-4-10, Koraibashi, CHUO KU OSAKA 541-0043, JP

Establishment Type(s)

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

Owner / Operator

LIVEDO CORPORATION (Owner Number: 9030441)

Owner / Operator Contact Address

Yodoyabashi Center Bldg. 8F-9F, 3-4-10, Koraibashi, CHUO KU OSAKA, JP-27 541-0043, JP

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Refre

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
EYQ	Garment, Protective, For Incontinence	Gastroenterology, Urology	Class 1	876.5920	2006-04-06

Official Correspondent

TAKASHI OGINO

US Agent Details

TAKUYA HISHIKAWA Business: LIVEDO USA, INC. Email: hishikawa959@livedo.jp Phone: (252) 2371373

Related Public Records

Same Entity

LIVEDO CORPORATION

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 3005674561. Last updated year: 2026. Please use registration number 3005674561 when referencing this establishment in official correspondence.