Consulting Wallah › Device Explorer › Ophthalmic › Intraocular scissors, probe-like, reusable
Device Explorer · FDA GUDID · GMDN 63486

Intraocular scissors, probe-like, reusable

A hand-held, manual, ophthalmic surgical instrument intended to be used to cut intraocular tissue (e.g., during anterior chamber surgery, vitrectomy). As a complete instrument it comprises two shearing blades at the end of a probe-/cannula-like shaft with a pr

US‑registered devices146in commercial distribution
Companies10labelers on GUDID
Single‑use0%of device records
Sterile0%labelled sterile
Prescription42%Rx‑only share
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Share of device records

Rumex International Corp.6545%
Katena Products, Inc.3323%
Geuder Aktiengesellschaft118%
Eye Technology Limited107%
D.O.R.C. Dutch Ophthalmic Research Center (International) B.V.107%
Krishna Imports Inc75%
Sontec Instruments, Inc.43%
Med Saver, Inc.32%

Top labelers

CompanyDevicesShare
Rumex International Corp.6545%
Katena Products, Inc.3323%
Geuder Aktiengesellschaft118%
Eye Technology Limited107%
D.O.R.C. Dutch Ophthalmic Research Center (International) B.V.107%
Krishna Imports Inc75%
Sontec Instruments, Inc.43%
Med Saver, Inc.32%
A1 Medical Gmbh21%
Duckworth And Kent Limited11%

Company = labeler of record on GUDID. 10 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

Eye TechnologyDuckworth & KentGerten Iridectomy ScissorVitrectomy ScissorsN.A.Lens LoopOph.ScissorsZALDIVAR IRIDECTOMY SCISSORSKAWAI HORIZONTAL SCISSORS 25 GAUGEYAE SCISSORSVRTIS CURVED SCISSORS 27 GAUGEVRTIS VERTICAL SCISSORS 25 GAUGEVRTIS CURVED SCISSORS 25 GAUGEHATA 25 GAUGE SCISSORSVRTIS HORIO PICK/SCISSORS 25 GAUGE23 GAUGE KUSAKA NON TROCAR VERT SCIS

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

FDA product codes

CodeNameDevices
HNFScissors, Ophthalmic91
HNFSCISSORS, OPHTHALMIC58

GMDN & GCC registration

  • GMDN code 63486 · non‑implantable
  • Single‑use 0% · sterile 0% · Rx‑only 42% · 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 intraocular scissors, probe-like, reusable products are registered in the US?

146 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Intraocular scissors, probe-like, reusable", from 10 companies. The largest labeler is Rumex International Corp. with 45% of records.

Which FDA product codes apply?

HNF (Scissors, Ophthalmic), HNF (SCISSORS, 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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