An electrically-powered device assembly intended to apply various modes of electrical stimulation transcutaneously to treat/prevent neuromuscular symptoms and disorders typically as a form of physical therapy [neuromuscular electrical stimulation (NMES)/electr
| Company | Devices | Share |
|---|---|---|
| Hong Qiangxing (Shen Zhen) Electronics Limited | 518 | 25% |
| Motive Health, Inc. | 191 | 9% |
| Nuface | 109 | 5% |
| Drive Devilbiss Healthcare | 96 | 5% |
| Everyway Medical Instruments Co., Ltd. | 79 | 4% |
| Healthmate International,Llc | 69 | 3% |
| Djo, Llc | 53 | 3% |
| Hi-Dow International Incorporated | 51 | 2% |
| Shenzhen Jian Feng Electronic Technology Co., Ltd. | 48 | 2% |
| Shanghai Youwen Medical Technology Co.,Ltd. | 43 | 2% |
| Shenzhen As-Tec Technology Co.,Ltd. | 42 | 2% |
| Syrma Johari Medtech Limited | 31 | 2% |
Company = labeler of record on GUDID. 148 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 |
|---|---|---|
| GZJ | Stimulator, Nerve, Transcutaneous, For Pain Relief | 815 |
| NGX | Stimulator, Muscle, Powered, For Muscle Conditioning | 578 |
| IPF | Stimulator, Muscle, Powered | 504 |
| NUH | Stimulator, Nerve, Transcutaneous, Over-The-Counter | 490 |
| KQX | Goniometer, Ac-Powered | 101 |
| GZI | Stimulator, Neuromuscular, External Functional | 81 |
Use these as the dimensions to specify in a tender line.
2,055 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Physical therapy transcutaneous neuromuscular electrical stimulation system", from 148 companies. The largest labeler is Hong Qiangxing (Shen Zhen) Electronics Limited with 25% of records.
GZJ (Stimulator, Nerve, Transcutaneous, For Pain Relief), NGX (Stimulator, Muscle, Powered, For Muscle Conditioning), IPF (Stimulator, Muscle, Powered), NUH (Stimulator, Nerve, Transcutaneous, Over-The-Counter)
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.