Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3001224205

FEI Number

3001224205

Entity Name

YA-MAN LTD.

City/State/Country

Koto-ku Tokyo, JP

Establishment Address

1-4-4 Furuishiba, Koto-ku Tokyo 135-0045, JP

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility,Export Device to the United States But Perform No Other Operation on Device

Owner / Operator

YA-MAN LTD. (Owner Number: 10039976)

Owner / Operator Contact Address

Shingu bldg. 4th floor, 2-4-2 Toyo, Koto-ku, JP-13 135-0016, JP

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K250618

PMA Number

N/A

All Registered Proprietary Names

L-SER KO YA-MAN LTD. Medi Lift Essential Medi Lift Pro Medi Lift Essential Eye Mask

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
ILY	Lamp, Infrared, Therapeutic Heating	Physical Medicine	Class 2	890.5500	2012-02-26
NUH	Stimulator, Nerve, Transcutaneous, Over-The-Counter	Neurology	Class 2	882.5890	2013-04-26
NHN	Powered Light Based Laser Non-Thermal Instrument With Non-Heating Effect For Adjunctive Use In Pain Therapy	Physical Medicine	Class 2	890.5500	2013-04-26
NFO	Stimulator, Transcutaneous Electrical, Aesthetic Purposes	Neurology	Class 2	882.5890	2023-07-10
NFO	Stimulator, Transcutaneous Electrical, Aesthetic Purposes	Neurology	Class 2	882.5890	2025-12-19

Official Correspondent

Izumi Maruo

US Agent Details

DAISUKE MASUYAMA Business: YA-MAN U.S.A. LTD Email: contactus@ya-man.com Phone: (858) 3504239

Related Public Records

Same Entity

YA-MAN LTD.

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

View Entity Profile →

Other Registrations for Same Entity

Registration Number	Establishment Name	Location
3039394880	KETAKA ELECTRIC Co.,Ltd.	Tottori, JP

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3001224205. Last updated year: 2026. Please use registration number 3001224205 when referencing this establishment in official correspondence.