J Mode (Shenzhen) Ltd (ACTMAN CORPORATION)

FDA Device Registration & Listing · Shenzhen City Guangdong, CN · Registration 9617420

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
9617420
FEI Number
3002926779
Entity Name
J Mode (Shenzhen) Ltd (ACTMAN CORPORATION)
City/State/Country
Shenzhen City Guangdong, CN
Establishment Address
No.6, Zhukeng Dier Industrial Zone,, Zhukeng Community, Pingshan New District, Shenzhen City Guangdong 518118, CN
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Topic Development Corporation (Owner Number: 9031872)
Owner / Operator Contact Address
7F-3, NO.129, Lane 235, Bauchiau Rd., Hsin Tien, TW-TPE 231, TW
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Twin Ball Facial Massager BP-346 Glitter Massage Roller, BP-365 Massager BP-390 Shampoo Brush AP-495 Wood Handle Massager BP-386 Massager, Electric

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LYG Massager, Therapeutic, Manual Physical Medicine Class 1 890.5660 1997-10-10
ISA Massager, Therapeutic, Electric Physical Medicine Class 1 890.5660 2000-10-02
HOY Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear) Ophthalmic Class 1 886.4750 1999-05-17

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

Topic Development 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 9617420. Last updated year: 2026. Please use registration number 9617420 when referencing this establishment in official correspondence.
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