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Device Explorer · FDA GUDID · GMDN 32556

Depth electrode

An electrical conductor intended to be temporarily placed (< 30 days) beneath the surface of the brain to stimulate the brain or to record the brain's electrical activity (with more precise localization than a scalp electrode). It is typically a fine, flexible

US‑registered devices1,440in commercial distribution
Companies7labelers on GUDID
Single‑use87%of device records
Sterile59%labelled sterile
Prescription99%Rx‑only share
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Share of device records

Pmt Corporation66546%
Alpha Omega Engineering Co. Ltd.25818%
Ad-Tech Medical Instrument Corporation22115%
Fhc, Inc.17112%
Dixi Medical977%
Neuroone Medical Technologies Corporation181%
Senso Medical Labs Ltd101%

Top labelers

CompanyDevicesShare
Pmt Corporation66546%
Alpha Omega Engineering Co. Ltd.25818%
Ad-Tech Medical Instrument Corporation22115%
Fhc, Inc.17112%
Dixi Medical977%
Neuroone Medical Technologies Corporation181%
Senso Medical Labs Ltd101%

Company = labeler of record on GUDID. 7 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

HaGuide SoftwareBengun AdapterBengun W/O ScrewsRemote ControlNeuro Omega Drive HeadstageNeuroNav Drive HeadstageNeuroSmart Autoclavable Drive HeadstageAutoclavable DriveNeuro Omega Autoclavable Drive HeadstagePower cableNeuroSmart NeuroForits Drive HeadstageNeuro Omega NeuroFortis Drive HeadstageNeuroNav MER HeadstageNeuroSmart MER HeadstageNeuro Omega MER HeadstageSterile neuroprobe

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

FDA product codes

CodeNameDevices
GZLElectrode, Depth1,070
GZLELECTRODE, DEPTH416
GYCELECTRODE, CORTICAL11
HAWNeurological stereotaxic Instrument7
GXIProbe, Radiofrequency Lesion5
GLZAntigens, If, Toxoplasma Gondii1

GMDN & GCC registration

  • GMDN code 32556 · non‑implantable
  • Single‑use 87% · sterile 59% · Rx‑only 99% · 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 (Millimeter) · 487Outer Diameter (Millimeter) · 306Length (Centimeter) · 58Needle Gauge (Gauge) · 24Length (Meter) · 2Lumen/Inner Diameter (Millimeter) · 2

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

No closely related category with 50+ devices.

How many depth electrode products are registered in the US?

1,440 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Depth electrode", from 7 companies. The largest labeler is Pmt Corporation with 46% of records.

Which FDA product codes apply?

GZL (Electrode, Depth), GZL (ELECTRODE, DEPTH), GYC (ELECTRODE, CORTICAL), HAW (Neurological stereotaxic Instrument)

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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