TENS PLUS INDUSTRIAL CO.

FDA Device Registration & Listing · HONG KONG, HK · Registration 3003836669

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
3003836669
FEI Number
3003836669
Entity Name
TENS PLUS INDUSTRIAL CO.
City/State/Country
HONG KONG, HK
Establishment Address
3/F., C12, WING HING IND. BLDG., 14, HING YIP ST. KWUN TONG, KOWLOON, HONG KONG NONE, HK
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
TENS PLUS INDUSTRIAL CO. (Owner Number: 9049984)
Owner / Operator Contact Address
3/F., C12, WING HING IND. BLDG., 14, HING YIP ST. KWUN TONG, KOWLOON, HONG KONG, HK-NOTA NONE, HK
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

POINTER EXCEL II-LT POINTER EXCEL II POINTER EXCEL AWQ-104LT AWQ-104L Pointer Pal Point Mate E-Stim II E-Stim III POINTER PLUS-LT POINTER PLUS Axus Es-5 Electro-Acupuncture Device

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief Neurology Class 2 882.5890 2011-12-01
GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief Neurology Class 2 882.5890 2011-12-01
BWJ Locator, Acupuncture Point General Hospital Class 2 880.5580 2022-10-28
GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief Neurology Class 2 882.5890 2011-01-20
GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief Neurology Class 2 882.5890 2011-12-01
BWK Stimulator, Electro-Acupuncture Unknown Class U N/A 2021-02-24

Official Correspondent

CLARA LAU

US Agent Details

Matthew Pike Business: Lhasa OMS, Inc. Email: mpikeoms@aol.com Phone: (781) 3401010

Related Public Records

Same Entity

TENS PLUS INDUSTRIAL CO.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K122948 Gemore Technology Co, Ltd. GEM-STIM COMBO STIMULATOR 2012-12-21
K033455 Biomedical Life Systems, Inc. ELECTRO-NERVE STIMULATOR TENS, MODEL BMLS03-5 2004-01-15
K810593 Medical Devices, Inc. NEUROPAC ULTRA I 1981-03-13

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3003836669. Last updated year: 2026. Please use registration number 3003836669 when referencing this establishment in official correspondence.
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