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Device Explorer · FDA GUDID · GMDN 47929

Lacrimal intubation set

A collection of devices intended to be used to maintain patency of the nasolacrimal system typically for treating/preventing pathologies of the tear drainage system (e.g., post-chemotherapy stenosis) or after dacryocystorhinostomy (DCR). It consists of a long

US‑registered devices57in commercial distribution
Companies11labelers on GUDID
Single‑use79%of device records
Sterile77%labelled sterile
Prescription89%Rx‑only share
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Share of device records

Katena Products, Inc.814%
Psi/Eye-Ko, Inc.814%
Jedmed Instrument Company814%
Fci S A S Fci 20 22712%
Surgistar, Inc.611%
Oasis Medical, Inc.611%
Quest Medical Inc611%
Beaver-Visitec International, Inc.35%

Top labelers

CompanyDevicesShare
Katena Products, Inc.814%
Psi/Eye-Ko, Inc.814%
Jedmed Instrument Company814%
Fci S A S Fci 20 22712%
Surgistar, Inc.611%
Oasis Medical, Inc.611%
Quest Medical Inc611%
Beaver-Visitec International, Inc.35%
Steris Corporation35%
Manus Medical, Llc12%
Novo Surgical, Inc.12%

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

Brand names on the register (sample)

SURGISTARDisposable InstrumentsLacrimal lntubation SetASICO LACRIMAL INTUBATION SETCRAWFORD LAC INTUB SET PROBE WITH TUBINGCATALANA LACRIMAL INTUBATION SETProbes, LacrimalLacrimal ProbeAnodyne SurgicalCustom Healthcare Systems Inc.Visitec®LacriCATHLACRIJET® 50LACRIJET® 45LACRIJET® 40LACRIJET® 35

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

FDA product codes

CodeNameDevices
OKSLacrimal Stents And Intubation Sets50
HNLProbe, lachrymal12
HNLProbe, Lachrymal3
HRHTrephine, Manual, Ophthalmic1
OJKEye Tray1

GMDN & GCC registration

  • GMDN code 47929 · non‑implantable
  • Single‑use 79% · sterile 77% · Rx‑only 89% · 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 (Inch) · 1

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

How many lacrimal intubation set products are registered in the US?

57 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Lacrimal intubation set", from 11 companies. The largest labeler is Katena Products, Inc. with 14% of records.

Which FDA product codes apply?

OKS (Lacrimal Stents And Intubation Sets), HNL (Probe, lachrymal), HNL (Probe, Lachrymal), HRH (Trephine, Manual, Ophthalmic)

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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