Consulting Wallah › Device Explorer › Other devices › Dermal curette, single-use
Device Explorer · FDA GUDID · GMDN 63259

Dermal curette, single-use

A hand-held manual surgical instrument designed exclusively for the precise scraping and/or excising of skin/dermal tissue (e.g., for treatment of superficial warts or wounds). It is available in a variety of shapes/sizes and has an appropriately-shaped distal

US‑registered devices417in commercial distribution
Companies22labelers on GUDID
Single‑use14%of device records
Sterile12%labelled sterile
Prescription22%Rx‑only share
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Share of device records

George Tiemann & Co.17943%
Sklar Corporation7318%
Hayden Medical, Inc.338%
Br Surgical, Llc266%
Ambler Surgical Corp.256%
Boss Instruments, Ltd., Inc.123%
Medipoint Holdings Llc92%
American Medicals92%

Top labelers

CompanyDevicesShare
George Tiemann & Co.17943%
Sklar Corporation7318%
Hayden Medical, Inc.338%
Br Surgical, Llc266%
Ambler Surgical Corp.256%
Boss Instruments, Ltd., Inc.123%
Medipoint Holdings Llc92%
American Medicals92%
Acuderm, Inc.82%
Robbins Instruments Inc.61%
Dynarex Corporation51%
Applied Dental, Inc.51%

Company = labeler of record on GUDID. 22 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

nexoderm® Dermal Curette Ø 7,0mmnexoderm® Dermal Curette Ø 4,0mmBOSS InstrumentsEVER READY SPLINTER OUT REMOVERN/AHayden MedicalBR Surgical, LLCCurPro Dermal Curettes, 7 mmCurPro Dermal Curettes, 5 mmCurPro Dermal Curettes, 4 mmCurPro Dermal Curettes, 3 mmCurPro Dermal Curettes,2 mmSHARDAcu-Dispo-CuretteROYAL TEKACME UNITED SPLINTER OUT

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

FDA product codes

CodeNameDevices
HTFCURETTE215
FZSCURETTE, SURGICAL, GENERAL USE76
FZSCurette, Surgical, General Use56
JYGCURETTE, EAR18
MDMINSTRUMENT, MANUAL, SURGICAL, GENERAL USE12
HTFCurette11

GMDN & GCC registration

  • GMDN code 63259 · non‑implantable
  • Single‑use 14% · sterile 12% · Rx‑only 22% · OTC 5%
  • 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) · 1

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

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

417 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Dermal curette, single-use", from 22 companies. The largest labeler is George Tiemann & Co. with 43% of records.

Which FDA product codes apply?

HTF (CURETTE), FZS (CURETTE, SURGICAL, GENERAL USE), FZS (Curette, Surgical, General Use), JYG (CURETTE, EAR)

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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