Device Explorer · FDA GUDID · GMDN 16025

Eye spud

A hand-held, manual, ophthalmic surgical instrument intended to be used to remove a foreign body/object embedded in or adhering to the surface of the eye globe. It is typically made of high-grade stainless steel, and designed with a fine handle at the proximal

US‑registered devices131in commercial distribution
Companies21labelers on GUDID
Single‑use4%of device records
Sterile2%labelled sterile
Prescription84%Rx‑only share
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Share of device records

Avalign Technologies, Inc.4534%
Ambler Surgical Corp.129%
Novo Surgical, Inc.108%
Med Saver, Inc.108%
Katena Products, Inc.97%
Integra Lifesciences Production Corporation97%
Krishna Imports Inc65%
Sontec Instruments, Inc.65%

Top labelers

CompanyDevicesShare
Avalign Technologies, Inc.4534%
Ambler Surgical Corp.129%
Novo Surgical, Inc.108%
Med Saver, Inc.108%
Katena Products, Inc.97%
Integra Lifesciences Production Corporation97%
Krishna Imports Inc65%
Sontec Instruments, Inc.65%
Teleflex Incorporated43%
Steris Corporation43%
Steris Deutschland Gmbh32%
Walcott Rx Product Inc22%

Company = labeler of record on GUDID. 21 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

Quire ear foreign body leverAESCULAPIntrace USASpudNovo Surgical Inc.ELLIS FOREIGN BODY SPUDFRANCIS FOREIGN BODY SPUDGOLF CLUB FOREIGN BODY SPUDWalcott Rx ProductsStephens InstrumentsV. MuellerMSI Precision Specialty InstrumentsForeign Body SpudDRYSDALE NUCLEUS MANIPULATORGOLEFT CLUB FOREIGN BODY SPUDMillennium

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

FDA product codes

CodeNameDevices
HNASpud, ophthalmic66
HNDSpatula, ophthalmic27
HNASpud, Ophthalmic11
JYTPICK, MICROSURGICAL EAR8
HNDSpatula, Ophthalmic8
HNNKnife, ophthalmic7

GMDN & GCC registration

  • GMDN code 16025 · non‑implantable
  • Single‑use 4% · sterile 2% · Rx‑only 84% · 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 eye spud products are registered in the US?

131 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Eye spud", from 21 companies. The largest labeler is Avalign Technologies, Inc. with 34% of records.

Which FDA product codes apply?

HNA (Spud, ophthalmic), HND (Spatula, ophthalmic), HNA (Spud, Ophthalmic), JYT (PICK, MICROSURGICAL EAR)

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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