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Device Explorer · FDA GUDID · GMDN 46871

Endometrial biopsy curette

A hand-held, surgical instrument used to for the removal of small amounts of endometrial secretions and/or tissue from the uterus for biopsy purposes. It is typically made of high-grade stainless steel and is available in a variety of designs: 1) a long, thin,

US‑registered devices133in commercial distribution
Companies17labelers on GUDID
Single‑use6%of device records
Sterile6%labelled sterile
Prescription69%Rx‑only share
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Share of device records

Gimmi Gmbh4635%
Gynex Corporation3123%
Coopersurgical, Inc.1713%
Schobell Industrial Ltda1310%
American Medicals65%
Teleflex Incorporated43%
Premier Dental Products Company32%
Uvision 360, Inc.22%

Top labelers

CompanyDevicesShare
Gimmi Gmbh4635%
Gynex Corporation3123%
Coopersurgical, Inc.1713%
Schobell Industrial Ltda1310%
American Medicals65%
Teleflex Incorporated43%
Premier Dental Products Company32%
Uvision 360, Inc.22%
Steris Corporation22%
Utah Medical Products, Inc.22%
Olympus Winter & Ibe Gmbh11%
Gyrus Acmi, Llc11%

Company = labeler of record on GUDID. 17 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

GimmiOlympusSims CuretteSims CurretteLondon CuretteEndocrette CuretteTownsend CuretteKevorkian CuretteKevorkian Collector CuretteRandall CuretteNovak CuretteEndocervical CuretteLUMINELLE Bx 360° Rotatable Disposable Sheath (BVacurettePremierMSI Precision Specialty Instruments

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

FDA product codes

CodeNameDevices
HCYCurette, Uterine66
FZSCurette, Surgical, General Use32
HHKCurette, Suction, Endometrial (And Accessories)8
HCYCURETTE, UTERINE7
LXHOrthopedic Manual Surgical Instrument6
GACRasp, Surgical, General & Plastic Surgery3

GMDN & GCC registration

  • GMDN code 46871 · non‑implantable
  • Single‑use 6% · sterile 6% · Rx‑only 69% · OTC 1%
  • UAE: MOHAP / DoH medical device registration and an authorised representative are required; Saudi: SFDA MDMA. We check status on request.

Size attributes recorded

Length (Millimeter) · 14Outer Diameter (Millimeter) · 11Length (Centimeter) · 2Length (Inch) · 1

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

How many endometrial biopsy curette products are registered in the US?

133 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Endometrial biopsy curette", from 17 companies. The largest labeler is Gimmi Gmbh with 35% of records.

Which FDA product codes apply?

HCY (Curette, Uterine), FZS (Curette, Surgical, General Use), HHK (Curette, Suction, Endometrial (And Accessories)), HCY (CURETTE, UTERINE)

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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