An assembly of electrically-powered devices designed to reduce the perception of pain by electrically stimulating peripheral nerves across the skin [transcutaneous electrical nerve stimulation (TENS)]. It includes an external current generator and skin-surface
| Company | Devices | Share |
|---|---|---|
| Shenzhen Yuwen E-Commerce Co., Ltd. | 130 | 18% |
| Gemore Technology Co., Ltd. | 118 | 17% |
| Shenzhen Kentro Medical Electronics Co.,Ltd | 79 | 11% |
| Avazzia Inc | 26 | 4% |
| Adp Health Limited | 23 | 3% |
| Neurometrix, Inc. | 23 | 3% |
| Hong Qiangxing (Shen Zhen) Electronics Limited | 18 | 3% |
| Uan Healthcare Limited | 16 | 2% |
| Shenzhen Sinrel Tech Ltd | 13 | 2% |
| Sublimed | 13 | 2% |
| Biomedical Life Systems, Inc. | 13 | 2% |
| Micro Current Technology, Inc. | 12 | 2% |
Company = labeler of record on GUDID. 84 companies in total; top 12 shown. Click headers to sort.
Sample of brand names as labelled; no endorsement. Ask us for the full list with company, model and UDI.
| Code | Name | Devices |
|---|---|---|
| NUH | Stimulator, Nerve, Transcutaneous, Over-The-Counter | 466 |
| NGX | Stimulator, Muscle, Powered, For Muscle Conditioning | 316 |
| GZJ | Stimulator, Nerve, Transcutaneous, For Pain Relief | 212 |
| IPF | Stimulator, Muscle, Powered | 94 |
| NYN | Stimulator, Electrical, Transcutaneous, For Arthritis | 56 |
| LIH | Interferential Current Therapy | 23 |
Use these as the dimensions to specify in a tender line.
708 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Analgesic transcutaneous electrical nerve stimulation system", from 84 companies. The largest labeler is Shenzhen Yuwen E-Commerce Co., Ltd. with 18% of records.
NUH (Stimulator, Nerve, Transcutaneous, Over-The-Counter), NGX (Stimulator, Muscle, Powered, For Muscle Conditioning), GZJ (Stimulator, Nerve, Transcutaneous, For Pain Relief), IPF (Stimulator, Muscle, Powered)
No. GUDID is the US register. For the UAE (MOHAP/DoH) and Saudi (SFDA/MDMA) a separate registration and a local authorised representative are required; Consulting Wallah can check the status and connect you with registered suppliers.
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Source: FDA AccessGUDID (AccessGUDID full release 2 Nov 2026); counts are device records in commercial distribution grouped by GMDN preferred term; companies are labelers of record. Information only — US listing is not a registration in the UAE or GCC; verify with the regulator. © Consulting Wallah — CC BY‑NC‑ND.