A non-sterile, hand-held, pen-like electrical conductor intended to be held against a patient's skin (noninvasive) to provide therapeutic electrical stimuli through the body surface [e.g., transcutaneous electrical nerve stimulation (TENS), electrical muscle s
| Company | Devices | Share |
|---|---|---|
| Shenzhen Roundwhale Technology Co. Ltd. | 32 | 50% |
| Shenzhen Jianchao Intelligent Technology Co., Ltd | 9 | 14% |
| Electromedical Products International, Inc. | 4 | 6% |
| Shenzhen Dachi Communication Co.,Ltd | 3 | 5% |
| Truerelief, Llc | 3 | 5% |
| Djo, Llc | 2 | 3% |
| Beijing Choice Electronic Technology Co., Ltd. | 2 | 3% |
| Septodont, Inc. | 2 | 3% |
| Inmode M.D Ltd | 1 | 2% |
| Everyway Medical Instruments Co., Ltd. | 1 | 2% |
| Biosonic Technologies Llc | 1 | 2% |
| Bioness Inc. | 1 | 2% |
Company = labeler of record on GUDID. 15 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 | 31 |
| GZJ | Stimulator, Nerve, Transcutaneous, For Pain Relief | 22 |
| IPF | Stimulator, Muscle, Powered | 21 |
| NGX | Stimulator, Muscle, Powered, For Muscle Conditioning | 19 |
| NFO | Stimulator, Transcutaneous Electrical, Aesthetic Purposes | 16 |
| OHS | Light Based Over The Counter Wrinkle Reduction | 13 |
Use these as the dimensions to specify in a tender line.
64 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Transcutaneous electrical stimulation probe", from 15 companies. The largest labeler is Shenzhen Roundwhale Technology Co. Ltd. with 50% of records.
NUH (Stimulator, Nerve, Transcutaneous, Over-The-Counter), GZJ (Stimulator, Nerve, Transcutaneous, For Pain Relief), IPF (Stimulator, Muscle, Powered), NGX (Stimulator, Muscle, Powered, For Muscle Conditioning)
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.