A hand-held instrument intended to be used to illuminate sinus tissue during an ear/nose/throat (ENT) procedure to render the tissue translucent for examination. It is connected through a light cable, that may or may not be part of the device, to a light sourc
| Company | Devices | Share |
|---|---|---|
| Integra Microfrance | 53 | 85% |
| Fentex Medical Gmbh | 4 | 6% |
| Practicon, Inc. | 2 | 3% |
| Stryker Corporation | 1 | 2% |
| U.S. Ophthalmic, L.L.C. | 1 | 2% |
| Sontec Instruments, Inc. | 1 | 2% |
Company = labeler of record on GUDID. 6 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 |
|---|---|---|
| CCW | LARYNGOSCOPE, RIGID | 32 |
| EQH | SOURCE, CARRIER, FIBEROPTIC LIGHT | 24 |
| HJN | Transilluminator, Battery-Powered | 3 |
| KAL | RETRACTOR, ENT | 1 |
| EPY | SPECULUM, ENT | 1 |
| LRC | Instrument, Ent Manual Surgical | 1 |
Use these as the dimensions to specify in a tender line.
62 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "ENT transilluminator", from 6 companies. The largest labeler is Integra Microfrance with 85% of records.
CCW (LARYNGOSCOPE, RIGID), EQH (SOURCE, CARRIER, FIBEROPTIC LIGHT), HJN (Transilluminator, Battery-Powered), KAL (RETRACTOR, ENT)
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.