Consulting Wallah › Device Explorer › Other devices › Percutaneous radio-frequency ablation probe, dener
Device Explorer · FDA GUDID · GMDN 62025

Percutaneous radio-frequency ablation probe, denervation, monopolar, reusable

A semi-flexible, hand-held surgical instrument intended to be percutaneously introduced via a dedicated cannula [under x-ray, ultrasound (US) or other external image guidance] to deliver radio-frequency current, in a monopolar configuration, from a system gene

US‑registered devices208in commercial distribution
Companies11labelers on GUDID
Single‑use12%of device records
Sterile4%labelled sterile
Prescription71%Rx‑only share
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Share of device records

Avanos Medical, Inc.7737%
Diros Technology Inc6029%
Minta Medical Limited178%
Neurotherm, Inc.105%
St. Jude Medical, Inc.84%
Lccs Products Limited84%
Marina Medical Instruments, Inc.84%
Stratus Medical Llc63%

Top labelers

CompanyDevicesShare
Avanos Medical, Inc.7737%
Diros Technology Inc6029%
Minta Medical Limited178%
Neurotherm, Inc.105%
St. Jude Medical, Inc.84%
Lccs Products Limited84%
Marina Medical Instruments, Inc.84%
Stratus Medical Llc63%
Medtronic Sofamor Danek, Inc.63%
Stryker Corporation42%
Italian Engineering Srl42%

Company = labeler of record on GUDID. 11 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

MULTIGEN 2NANeuroTherm™EpimedRF THERMOCOUPLE ELECTRODENimbus Probe (Reusable)LCCSMarina MedicalOWLAccurianAVANOSCOOLIEF* Multi-Cooled Radiofrequency KitHalyard

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

FDA product codes

CodeNameDevices
GXIPROBE, RADIOFREQUENCY LESION103
GXIProbe, Radiofrequency Lesion71
GXIProbe, radiofrequency lesion28
EXXPROBE, RECTAL, NON-POWERED8
GXDGENERATOR, LESION, RADIOFREQUENCY4
GEIElectrosurgical, Cutting & Coagulation & Accessories4

GMDN & GCC registration

  • GMDN code 62025 · non‑implantable
  • Single‑use 12% · sterile 4% · Rx‑only 71% · 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) · 31Length (Millimeter) · 16Catheter Length (Millimeter) · 4Needle Gauge (Gauge) · 4Length (Inch) · 1

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

How many percutaneous radio-frequency ablation probe, denervation, monopolar, reusable products are registered in the US?

208 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Percutaneous radio-frequency ablation probe, denervation, monopolar, reusable", from 11 companies. The largest labeler is Avanos Medical, Inc. with 37% of records.

Which FDA product codes apply?

GXI (PROBE, RADIOFREQUENCY LESION), GXI (Probe, Radiofrequency Lesion), GXI (Probe, radiofrequency lesion), EXX (PROBE, RECTAL, NON-POWERED)

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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