MIXEN COMPANY LIMITED

FDA Device Registration & Listing · Kowloon, HK · Registration 3013510855

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
3013510855
FEI Number
3013510855
Entity Name
MIXEN COMPANY LIMITED
City/State/Country
Kowloon, HK
Establishment Address
Unit 390, 3/F., Peninsula Centre, 67 Mody Road, Tsim Sha Tsui East, Kowloon 999077, HK
Establishment Type(s)
Export Device to the United States But Perform No Other Operation on Device,Manufacture Medical Device
Owner / Operator
MIXEN COMPANY LIMITED (Owner Number: 10053270)
Owner / Operator Contact Address
Unit 390, 3/F., Peninsula Centre, 67 Mody Road, Tsim Sha Tsui East, Kowloon, HK-NOTA 999077, HK
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Lippo Massager, GLO910 PRO Lippo Massager, GLO910 Lippo Massager, GLO910+

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
ISA Massager, Therapeutic, Electric Physical Medicine Class 1 890.5660 2016-11-15

Official Correspondent

Ixone Elosegui

US Agent Details

Juan Tezak Business: Compliance4devices Email: juantezak@gmail.com Phone: (561) 7892411

Related Public Records

Same Entity

MIXEN COMPANY LIMITED
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 3013510855. Last updated year: 2026. Please use registration number 3013510855 when referencing this establishment in official correspondence.
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