An implantable short tube intended to provide a bypass route for tear drainage from the corner of the eye into the nasal cavity, or a paranasal sinus, as treatment for pathologies of the tear drainage system in association with functional or obstructive epipho
| Company | Devices | Share |
|---|---|---|
| Fci S A S Fci 20 22 | 64 | 85% |
| Kaneka Corporation | 4 | 5% |
| Rumex International Corp. | 4 | 5% |
| Stradis Medical, Llc | 3 | 4% |
Company = labeler of record on GUDID. 4 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 |
|---|---|---|
| OKS | Lacrimal Stents And Intubation Sets | 68 |
| GAZ | Tubing, Noninvasive | 4 |
| MIB | Elastomer, Silicone Block | 3 |
| LZU | Plug, Punctum | 1 |
Use these as the dimensions to specify in a tender line.
No closely related category with 50+ devices.
75 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Lacrimal tube", from 4 companies. The largest labeler is Fci S A S Fci 20 22 with 85% of records.
OKS (Lacrimal Stents And Intubation Sets), GAZ (Tubing, Noninvasive), MIB (Elastomer, Silicone Block), LZU (Plug, Punctum)
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.