An electrically-powered, noninvasive device designed to generate radio-frequency (RF) electrical current used to create heat via a percutaneously (through the skin) introduced electrode(s) in a precise location, at a controlled temperature, for focal ablation
| Company | Devices | Share |
|---|---|---|
| Medtronic Sofamor Danek, Inc. | 23 | 13% |
| Smith & Nephew, Inc. | 17 | 9% |
| Biomet Orthopedics, Llc | 16 | 9% |
| Boston Scientific Neuromodulation Corporation | 12 | 7% |
| Inmode M.D Ltd | 10 | 6% |
| Celling Biosciences | 9 | 5% |
| Boston Scientific Corporation | 9 | 5% |
| Neuroone Medical Technologies Corporation | 8 | 4% |
| Avanos Medical, Inc. | 8 | 4% |
| Stockert Gmbh | 6 | 3% |
| Thermi | 6 | 3% |
| Stryker Corporation | 5 | 3% |
Company = labeler of record on GUDID. 34 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 |
|---|---|---|
| GEI | Electrosurgical, Cutting & Coagulation & Accessories | 51 |
| GEI | ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES | 35 |
| GEI | Electrosurgical, cutting & coagulation & accessories | 17 |
| GXD | Generator, lesion, radiofrequency | 16 |
| LZO | Prosthesis, hip, semi-constrained, metal/ceramic/polymer, ce | 16 |
| GXD | GENERATOR, LESION, RADIOFREQUENCY | 15 |
Use these as the dimensions to specify in a tender line.
180 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Percutaneous radio-frequency ablation system generator", from 34 companies. The largest labeler is Medtronic Sofamor Danek, Inc. with 13% of records.
GEI (Electrosurgical, Cutting & Coagulation & Accessories), GEI (ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES), GEI (Electrosurgical, cutting & coagulation & accessories), GXD (Generator, lesion, radiofrequency)
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.