Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3012441818

FEI Number

3012441818

Entity Name

ZUIKO MEDICAL CORPORATION

City/State/Country

Settsu-city Osaka, JP

Establishment Address

3-50 Torikaikami 4-chome, Settsu-city Osaka 566-0062, JP

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Zuiko Medical Corporation (Owner Number: 10050258)

Owner / Operator Contact Address

3-50 Torikaikami 4-chome, Settsu-city, JP-27 566-0062, JP

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Plus moist HSP Plus moist HSP-W Plus moist HS-W

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
NAC	Dressing, Wound, Hydrophilic	General, Plastic Surgery	Class 1	878.4018	2015-10-26

Official Correspondent

Kazuya Iwata

US Agent Details

Genta Yoshida Business: Zuiko Inc. Email: inquiry@zuikoinc.com Phone: (470) 7198316

Related Public Records

Same Entity

Zuiko Medical 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 3012441818. Last updated year: 2026. Please use registration number 3012441818 when referencing this establishment in official correspondence.