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Device Explorer · FDA GUDID · GMDN 65308

Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead extension

An implantable device intended to extend the electrical connection between a spinal cord/peripheral nerve implantable analgesic electrical stimulation system pulse generator and a lead(s). It typically includes small connectors to enable attachment to the lead

US‑registered devices50in commercial distribution
Companies5labelers on GUDID
Single‑use100%of device records
Sterile100%labelled sterile
Prescription92%Rx‑only share
ImplantableYesGMDN flag
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Share of device records

Medtronic, Inc.1938%
Boston Scientific Neuromodulation Corporation1428%
St. Jude Medical, Inc.918%
Nevro Corp.48%
Nalu Medical, Inc.48%

Top labelers

CompanyDevicesShare
Medtronic, Inc.1938%
Boston Scientific Neuromodulation Corporation1428%
St. Jude Medical, Inc.918%
Nevro Corp.48%
Nalu Medical, Inc.48%

Company = labeler of record on GUDID. 5 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

NAA127™SJM™Nevro®Nalu Medical, Inc.Precision™

Sample of brand names as labelled; no endorsement. Ask us for the full list with company, model and UDI.

FDA product codes

CodeNameDevices
LGWSTIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF66
QRBStimulator, spinal-cord, totally implanted for relief of pai26
GZFStimulator, Peripheral Nerve, Implanted (Pain Relief)10
LGWStimulator, Spinal-Cord, Totally Implanted For Pain Relief4
GZBStimulator, Spinal-Cord, Implanted (Pain Relief)4
PMPDorsal root ganglion stimulator for pain relief2

GMDN & GCC registration

  • GMDN code 65308 · implantable
  • Single‑use 100% · sterile 100% · Rx‑only 92% · OTC 0%
  • UAE: MOHAP / DoH medical device registration and an authorised representative are required; Saudi: SFDA MDMA. We check status on request.

Size attributes recorded

Length (Centimeter) · 50

Use these as the dimensions to specify in a tender line.

How many spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead extension products are registered in the US?

50 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 extension", from 5 companies. The largest labeler is Medtronic, Inc. with 38% of records.

Which FDA product codes apply?

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)

Is this the same as UAE/GCC registration?

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.

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