An assembly of mains electricity (AC-powered) devices intended for the relief of chronic neuropathic pain through percutaneous electrical nerve stimulation (PENS). It typically consists of external current generator, return electrode(s), connection cables and
| Company | Devices | Share |
|---|---|---|
| Spr Therapeutics, Inc. | 62 | 97% |
| Biowave Corporation | 1 | 2% |
| Bioventus Llc | 1 | 2% |
Company = labeler of record on GUDID. 3 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 |
|---|---|---|
| NHI | Stimulator, Nerve, Electrical, Percutaneous (Pens), For Pain | 93 |
| NHI | Stimulator, Nerve, Electrial, Percutaneous (Pens), For Pain | 25 |
| NIH | Disinfectant, Subsystem, Water Purification | 1 |
| GZF | Stimulator, Peripheral Nerve, Implanted (Pain Relief) | 1 |
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 "Analgesic PENS system", from 3 companies. The largest labeler is Spr Therapeutics, Inc. with 97% of records.
NHI (Stimulator, Nerve, Electrical, Percutaneous (Pens), For Pain), NHI (Stimulator, Nerve, Electrial, Percutaneous (Pens), For Pain ), NIH (Disinfectant, Subsystem, Water Purification), GZF (Stimulator, Peripheral Nerve, Implanted (Pain Relief))
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.