Consulting Wallah › Device Explorer › Other devices › Corneal marker handpiece
Device Explorer · FDA GUDID · GMDN 61740

Corneal marker handpiece

A manually-operated instrument intended to be used with a disposable handpiece tip (not included) to ink mark corneal tissue prior to an ophthalmic surgical procedure. It is a pen-like device with a weighted, self-levelling mechanism intended to accept the ink

US‑registered devices60in commercial distribution
Companies2labelers on GUDID
Single‑use0%of device records
Sterile0%labelled sterile
Prescription0%Rx‑only share
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Share of device records

Rashman Corporation5795%
Surgilum, Llc35%

Top labelers

CompanyDevicesShare
Rashman Corporation5795%
Surgilum, Llc35%

Company = labeler of record on GUDID. 2 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

PenlightRoboMarker G2RoboMarker-RefurbishedSurgilum

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

FDA product codes

CodeNameDevices
KYTLight, Examination, Medical, Battery Powered57
HMRMarker, Ocular3

GMDN & GCC registration

  • GMDN code 61740 · non‑implantable
  • Single‑use 0% · sterile 0% · Rx‑only 0% · 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

No structured size data on the register.

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

How many corneal marker handpiece products are registered in the US?

60 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Corneal marker handpiece", from 2 companies. The largest labeler is Rashman Corporation with 95% of records.

Which FDA product codes apply?

KYT (Light, Examination, Medical, Battery Powered), HMR (Marker, Ocular)

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.

How do I get quotes?

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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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