MEHOR JAPAN CO., LTD

FDA Device Registration & Listing · Osaka-shi, JP · Registration 3014165708

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3014165708
FEI Number
3014165708
Entity Name
MEHOR JAPAN CO., LTD
City/State/Country
Osaka-shi, JP
Establishment Address
4-2-26-808 Nishinakajima, Yodogawa-ku, Osaka-shi 5320011, JP
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Mehor Japan Co., Ltd (Owner Number: 10056357)
Owner / Operator Contact Address
4-2-26-808 Nishinakajima, Yodogawa-ku, Osaka-shi, JP-27 5320011, JP
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Health Care Mat Skin Pressure Protector

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
IKY Mattress, Flotation Therapy, Non-Powered General Hospital Class 1 880.5150 2017-12-01
FMP Protector, Skin Pressure General Hospital Class 1 880.6450 2017-12-01

Official Correspondent

No official correspondent registered.

US Agent Details

David Lennarz Business: Registrar corp Email: David.Lennarz@registrarcorp.com Phone: (757) 2240177

Related Public Records

Same Entity

Mehor Japan 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 3014165708. Last updated year: 2026. Please use registration number 3014165708 when referencing this establishment in official correspondence.
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