Consulting Wallah › Device Explorer › Other devices › Adenoid curette, single-use
Device Explorer · FDA GUDID · GMDN 63842

Adenoid curette, single-use

A sterile, 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

US‑registered devices55in commercial distribution
Companies3labelers on GUDID
Single‑use16%of device records
Sterile16%labelled sterile
Prescription100%Rx‑only share
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Share of device records

Integra Lifesciences Production Corporation4887%
Dtr Medical Limited47%
Medline Industries, Inc.35%

Top labelers

CompanyDevicesShare
Integra Lifesciences Production Corporation4887%
Dtr Medical Limited47%
Medline Industries, Inc.35%

Company = labeler of record on GUDID. 3 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

Beckmann Adenoid Curette, 17mm Curette Edge, 220Beckmann Adenoid Curette, 15mm Curette Edge, 220Beckmann Adenoid Curette, 13mm Curette Edge, 220Beckmann Adenoid Curette, 10mm Curette Edge, 220MedlineIntegra® Miltex®Integra® Jarit®Integra®

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

FDA product codes

CodeNameDevices
KBJCURETTE, ADENOID52
KBJCurette, Adenoid4

GMDN & GCC registration

  • GMDN code 63842 · non‑implantable
  • Single‑use 16% · sterile 16% · Rx‑only 100% · 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

Width (Millimeter) · 23Length (Inch) · 2

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

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

55 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Adenoid curette, single-use", from 3 companies. The largest labeler is Integra Lifesciences Production Corporation with 87% of records.

Which FDA product codes apply?

KBJ (CURETTE, ADENOID), KBJ (Curette, Adenoid)

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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