Consulting Wallah › Device Explorer › Endoscopy & surgical instruments › Corneal trephine manual instrument
Device Explorer · FDA GUDID · GMDN 32822

Corneal trephine manual instrument

A hand-held, ophthalmic surgical instrument, constructed as a one-piece handle with trephine (not an exchangeable component) that is manually rotated with downward pressure by a surgeon in order to cut and remove circular pieces of corneal tissue (corneal butt

US‑registered devices59in commercial distribution
Companies6labelers on GUDID
Single‑use14%of device records
Sterile14%labelled sterile
Prescription54%Rx‑only share
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Share of device records

Surtex Instruments Ltd.2746%
Moria Sa1831%
Beaver-Visitec International, Inc.712%
Bausch & Lomb Incorporated58%
Avalign Technologies, Inc.12%
Stradis Medical, Llc12%

Top labelers

CompanyDevicesShare
Surtex Instruments Ltd.2746%
Moria Sa1831%
Beaver-Visitec International, Inc.712%
Bausch & Lomb Incorporated58%
Avalign Technologies, Inc.12%
Stradis Medical, Llc12%

Company = labeler of record on GUDID. 6 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

SurtexMORIABeaver®BeaverBausch + LombMILLENNIUMSTRADIS HEALTHCARE

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

FDA product codes

CodeNameDevices
HRHTrephine, manual, ophthalmic28
HRHTrephine, Manual, Ophthalmic23
HNJPunch, Corneo-Scleral4
KDCInstrument, Surgical, Disposable3
HNDSpatula, Ophthalmic2
HNRForceps, Ophthalmic1

GMDN & GCC registration

  • GMDN code 32822 · non‑implantable
  • Single‑use 14% · sterile 14% · Rx‑only 54% · 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

Lumen/Inner Diameter (Millimeter) · 1

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No closely related category with 50+ devices.

How many corneal trephine manual instrument products are registered in the US?

59 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Corneal trephine manual instrument", from 6 companies. The largest labeler is Surtex Instruments Ltd. with 46% of records.

Which FDA product codes apply?

HRH (Trephine, manual, ophthalmic), HRH (Trephine, Manual, Ophthalmic), HNJ (Punch, Corneo-Scleral), KDC (Instrument, Surgical, Disposable)

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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