A mains electricity (AC-powered) assembly of devices intended to capture smoke generated during open surgical procedures involving tissue ablation (e.g., laser surgery, electrocautery, electrosurgical diathermy device). It captures the plume (smoke composed of
| Company | Devices | Share |
|---|---|---|
| Conmed Corporation | 46 | 19% |
| Medimax Tech Inc. | 33 | 14% |
| Deroyal Industries, Inc. | 29 | 12% |
| Acuderm, Inc. | 24 | 10% |
| I.C. Medical, Inc. | 21 | 9% |
| Megadyne Medical Products, Inc. | 17 | 7% |
| Cao Group, Inc. | 10 | 4% |
| Aspen Surgical Products, Inc. | 9 | 4% |
| Dermatologic Lab And Supply, Inc. | 8 | 3% |
| Medisourcenet, Inc | 7 | 3% |
| Coastal Life Technologies, Inc. | 6 | 3% |
| Coopersurgical, Inc. | 5 | 2% |
Company = labeler of record on GUDID. 23 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 |
|---|---|---|
| FYD | Apparatus, Exhaust, Surgical | 118 |
| FYD | APPARATUS, EXHAUST, SURGICAL | 70 |
| GEI | Electrosurgical, Cutting & Coagulation & Accessories | 33 |
| GEI | ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES | 23 |
| GEI | Electrosurgical, cutting & coagulation & accessories | 11 |
| EHZ | Evacuator, Oral Cavity | 10 |
Use these as the dimensions to specify in a tender line.
236 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Surgical plume evacuation system", from 23 companies. The largest labeler is Conmed Corporation with 19% of records.
FYD (Apparatus, Exhaust, Surgical), FYD (APPARATUS, EXHAUST, SURGICAL), GEI (Electrosurgical, Cutting & Coagulation & Accessories), GEI (ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES)
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.