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Device Explorer · FDA GUDID · GMDN 33449

Adenoid curette, reusable

A hand-held manual surgical instrument designed for cutting and excising adenoid tissue (hypertrophic lymphoid tissue in the nasopharynx) during an adenoidectomy (adenectomy). It is typically designed as a long, slender instrument with a handle at the proximal

US‑registered devices303in commercial distribution
Companies18labelers on GUDID
Single‑use3%of device records
Sterile0%labelled sterile
Prescription88%Rx‑only share
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Share of device records

Ambler Surgical Corp.3913%
Medicon Eg. Chirurgiemechaniker-Genossenschaft3813%
Novo Surgical, Inc.3311%
Sklar Corporation3311%
Spiggle & Theis Medizintechnik Gmbh3110%
Teleflex Incorporated217%
Med Saver, Inc.196%
Steris Corporation186%

Top labelers

CompanyDevicesShare
Ambler Surgical Corp.3913%
Medicon Eg. Chirurgiemechaniker-Genossenschaft3813%
Novo Surgical, Inc.3311%
Sklar Corporation3311%
Spiggle & Theis Medizintechnik Gmbh3110%
Teleflex Incorporated217%
Med Saver, Inc.196%
Steris Corporation186%
Bausch & Lomb Incorporated145%
Avalign Technologies, Inc.145%
Gimmi Gmbh93%
Sontec Instruments, Inc.83%

Company = labeler of record on GUDID. 18 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

Vogel adenoid curetteNegus adenoid curetteBeckmann adenoid curetteHalle antrum curetteStubbs adenoid curetteCoakley antrum curetteGimmiAESCULAPMediconNovo SurgicalNovo Surgical Inc.Hayden MedicalBR Surgical, LLCBausch + LombMSI Precision Specialty InstrumentsBarnhill Adenoid Curette

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

FDA product codes

CodeNameDevices
KBJCURETTE, ADENOID172
KBJCurette, Adenoid46
JYGCURETTE, EAR33
KAPCurette, Nasal14
KBHADENOTOME13
LRCINSTRUMENT, ENT MANUAL SURGICAL12

GMDN & GCC registration

  • GMDN code 33449 · non‑implantable
  • Single‑use 3% · sterile 0% · Rx‑only 88% · 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 (Inch) · 17

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

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

303 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Adenoid curette, reusable", from 18 companies. The largest labeler is Ambler Surgical Corp. with 13% of records.

Which FDA product codes apply?

KBJ (CURETTE, ADENOID), KBJ (Curette, Adenoid), JYG (CURETTE, EAR), KAP (Curette, Nasal)

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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