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Device Explorer · FDA GUDID · GMDN 65445

Endaural wax extraction curette

A hand-held, manual, non-surgical device intended to scrape within the ear canal primarily for the extraction of ear wax during an ear/nose/throat (ENT) procedure; it is not intended for surgical scraping or manipulation of tissues. It may have various designs

US‑registered devices57in commercial distribution
Companies7labelers on GUDID
Single‑use86%of device records
Sterile2%labelled sterile
Prescription26%Rx‑only share
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Share of device records

Medline Industries, Inc.1832%
American Hospital Supply Llc1221%
Bionix, Llc916%
Ear Technology Corporation916%
Black & Black Surgical, Inc.611%
Br Surgical, Llc24%
Trinity Sterile, Inc.12%

Top labelers

CompanyDevicesShare
Medline Industries, Inc.1832%
American Hospital Supply Llc1221%
Bionix, Llc916%
Ear Technology Corporation916%
Black & Black Surgical, Inc.611%
Br Surgical, Llc24%
Trinity Sterile, Inc.12%

Company = labeler of record on GUDID. 7 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

Safe Ear Curette™ Variety KitWhite FlexLoop®Yellow CeraSpoon®Blue InfantScoop®Purple VersaLoop®Red AngleLoop®Orange ControLoop®Green MicroLoop®American Hospital SupplyN/ABR Surgical, LLCLightBeamSample, Safe Ear Curette Rainbow PackMedlineTrinity Sterile, Inc.

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

FDA product codes

CodeNameDevices
JYGCURETTE, EAR33
JYGCurette, Ear19
JYQLoop, Wire2
FZSCURETTE, SURGICAL, GENERAL USE1

GMDN & GCC registration

  • GMDN code 65445 · non‑implantable
  • Single‑use 86% · sterile 2% · Rx‑only 26% · 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 endaural wax extraction curette products are registered in the US?

57 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Endaural wax extraction curette", from 7 companies. The largest labeler is Medline Industries, Inc. with 32% of records.

Which FDA product codes apply?

JYG (CURETTE, EAR), JYG (Curette, Ear), JYQ (Loop, Wire), FZS (CURETTE, SURGICAL, GENERAL USE)

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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