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Device Explorer · FDA GUDID · GMDN 47522

Endaural surgical curette, reusable

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 devices1,306in commercial distribution
Companies36labelers on GUDID
Single‑use2%of device records
Sterile1%labelled sterile
Prescription73%Rx‑only share
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Share of device records

Avalign Technologies, Inc.12610%
Marina Medical Instruments, Inc.1169%
Ambler Surgical Corp.1159%
Integra Lifesciences Production Corporation1048%
Sklar Corporation766%
Spiggle & Theis Medizintechnik Gmbh736%
Novo Surgical, Inc.645%
Boss Instruments, Ltd., Inc.584%

Top labelers

CompanyDevicesShare
Avalign Technologies, Inc.12610%
Marina Medical Instruments, Inc.1169%
Ambler Surgical Corp.1159%
Integra Lifesciences Production Corporation1048%
Sklar Corporation766%
Spiggle & Theis Medizintechnik Gmbh736%
Novo Surgical, Inc.645%
Boss Instruments, Ltd., Inc.584%
Br Surgical, Llc564%
Steris Corporation564%
Gsource Llc514%
Teleflex Incorporated504%

Company = labeler of record on GUDID. 36 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

EOSCuretteSpoon curetteSpoon curette,Buck ear curetteEar curetteFENTEXTisch micro curetteSpoon curette, semi-sharpMicro curetteHouse curette, double endedLempert mastoid curetteSpratt mastoid curetteRZ Medizintechnik GmbHn.a.AESCULAP

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

FDA product codes

CodeNameDevices
JYGCURETTE, EAR824
JYGCurette, Ear177
FZSCURETTE, SURGICAL, GENERAL USE77
JYQLOOP, WIRE74
LRCINSTRUMENT, ENT MANUAL SURGICAL56
FZSCurette, Surgical, General Use46

GMDN & GCC registration

  • GMDN code 47522 · non‑implantable
  • Single‑use 2% · sterile 1% · Rx‑only 73% · 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

Length (Centimeter) · 39Outer Diameter (Millimeter) · 35Length (Millimeter) · 33Length (Inch) · 30Width (Millimeter) · 11Angle (degree) · 3

Use these as the dimensions to specify in a tender line.

How many endaural surgical curette, reusable products are registered in the US?

1,306 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Endaural surgical curette, reusable", from 36 companies. The largest labeler is Avalign Technologies, Inc. with 10% of records.

Which FDA product codes apply?

JYG (CURETTE, EAR), JYG (Curette, Ear), FZS (CURETTE, SURGICAL, GENERAL USE), JYQ (LOOP, WIRE)

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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