An electrically-insulated wire with a distal electrode intended to be implanted into the epidural space of the spinal cord and/or in/near a peripheral nerve (e.g., lumbar, truncal, in a limb) for wired transmission of electrical impulses from a co-implanted pu
| Company | Devices | Share |
|---|---|---|
| St. Jude Medical, Inc. | 61 | 26% |
| Medtronic, Inc. | 49 | 21% |
| Boston Scientific Neuromodulation Corporation | 32 | 14% |
| Nalu Medical, Inc. | 24 | 10% |
| Advanced Neuromodulation Systems, Inc. | 20 | 9% |
| Nevro Corp. | 20 | 9% |
| Saluda Medical Pty Limited | 20 | 9% |
| Biotronik Se & Co. Kg | 4 | 2% |
| Neuros Medical, Inc. | 3 | 1% |
| Mainstay Medical Limited | 2 | 1% |
Company = labeler of record on GUDID. 10 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 |
|---|---|---|
| LGW | STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF | 224 |
| QRB | Stimulator, spinal-cord, totally implanted for relief of pai | 80 |
| GZF | Stimulator, Peripheral Nerve, Implanted (Pain Relief) | 51 |
| LGW | Stimulator, Spinal-Cord, Totally Implanted For Pain Relief | 43 |
| GZB | STIMULATOR, SPINAL-CORD, IMPLANTED (PAIN RELIEF) | 30 |
| LGW | Stimulator, spinal-cord, totally implanted for pain relief | 26 |
Use these as the dimensions to specify in a tender line.
235 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead, wired connection", from 10 companies. The largest labeler is St. Jude Medical, Inc. with 26% of records.
LGW (STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF), QRB (Stimulator, spinal-cord, totally implanted for relief of pai), GZF (Stimulator, Peripheral Nerve, Implanted (Pain Relief)), LGW (Stimulator, Spinal-Cord, Totally Implanted For 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.