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Device Explorer · FDA GUDID · GMDN 63876

Endaural surgical curette, single-use

A slender, hand-held, manual surgical instrument designed for procedures during middle ear surgery (e.g., removal of the superior bony rim), and may in addition be used for scraping within the ear canal (e.g., removing wax). The instrument has a serrated or bl

US‑registered devices58in commercial distribution
Companies11labelers on GUDID
Single‑use84%of device records
Sterile17%labelled sterile
Prescription14%Rx‑only share
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Share of device records

Sklar Corporation1933%
Medline Industries, Inc.814%
C F M Technologies Inc610%
Adept Medical Limited610%
Robinson Healthcare Limited59%
Mckesson Medical-Surgical Inc.59%
Owens & Minor Distribution, Inc.47%
Spiggle & Theis Medizintechnik Gmbh23%

Top labelers

CompanyDevicesShare
Sklar Corporation1933%
Medline Industries, Inc.814%
C F M Technologies Inc610%
Adept Medical Limited610%
Robinson Healthcare Limited59%
Mckesson Medical-Surgical Inc.59%
Owens & Minor Distribution, Inc.47%
Spiggle & Theis Medizintechnik Gmbh23%
Dtr Medical Limited12%
Exmoor Plastics Limited12%
Bioseal12%

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

Brand names on the register (sample)

House Curette, Double Ended 2.0/3.0mm Scoops, 18EXMOORInstrapacMENTIO disposable ear curette/cottonMENTIO disposable ear curette cottonCFM TechnologiesCFM TEechnologiesENT POCKET LIGHTBioseal Inc.SklarMediChoiceMedlineMEDLINEMcKessonAdept Medical Cerumen Management KitJobson Horne Probe - Oval, Sterile

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

FDA product codes

CodeNameDevices
JYGCURETTE, EAR31
JYGCurette, Ear18
JYHEXCAVATOR, EAR2
JYHExcavator, Ear2
ERAOtoscope2
LRCINSTRUMENT, ENT MANUAL SURGICAL1

GMDN & GCC registration

  • GMDN code 63876 · non‑implantable
  • Single‑use 84% · sterile 17% · Rx‑only 14% · OTC 16%
  • UAE: MOHAP / DoH medical device registration and an authorised representative are required; Saudi: SFDA MDMA. We check status on request.

Size attributes recorded

Length (Centimeter) · 5

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How many endaural surgical curette, single-use products are registered in the US?

58 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Endaural surgical curette, single-use", from 11 companies. The largest labeler is Sklar Corporation with 33% of records.

Which FDA product codes apply?

JYG (CURETTE, EAR), JYG (Curette, Ear), JYH (EXCAVATOR, EAR), JYH (Excavator, 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.

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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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