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Device Explorer · FDA GUDID · GMDN 66306

Neurosurgical curette, reusable

A hand-held manual surgical instrument intended to be used to scrape and debride tissue from a bone surface (e.g., cancellous vertebral bone of the spine) or a cavity wall during a neurosurgical procedure. It consists of a long, thin, metal shaft that terminat

US‑registered devices473in commercial distribution
Companies9labelers on GUDID
Single‑use0%of device records
Sterile0%labelled sterile
Prescription99%Rx‑only share
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Share of device records

Boss Instruments, Ltd., Inc.36778%
Spineology Inc.286%
Avalign Technologies, Inc.214%
Novo Surgical, Inc.194%
Integra Lifesciences Production Corporation112%
Genesys Orthopedics Systems Llc92%
Charmant Inc.61%
Adler, Inc.61%

Top labelers

CompanyDevicesShare
Boss Instruments, Ltd., Inc.36778%
Spineology Inc.286%
Avalign Technologies, Inc.214%
Novo Surgical, Inc.194%
Integra Lifesciences Production Corporation112%
Genesys Orthopedics Systems Llc92%
Charmant Inc.61%
Adler, Inc.61%
Sontec Instruments, Inc.61%

Company = labeler of record on GUDID. 9 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

BOSS InstrumentsMicro-Curette 0.75×1.5 80deg.Micro-Curette 1.5×2.0 30deg.Micro-Curette 1.0×2.0 80deg.Micro-Curette 0.75×1.0 80deg.Flat-Blade Micro-Ringcurette φ1.5Flat-Blade Micro-Ringcurette φ1.0Adler Instrument CompanyCURETTEBAYONET CURETTENEUROSURGICAL CURETTEBAYONET RING CURETTEMillenniumAvalignOptiMesh Multiplanar Expandable Interbody FusionDiscectomy Set

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

FDA product codes

CodeNameDevices
HAOINSTRUMENT, SURGICAL, NON-POWERED266
GZXINSTRUMENT, MICROSURGICAL89
FZSCURETTE, SURGICAL, GENERAL USE62
LXHOrthopedic Manual Surgical Instrument28
MAXIntervertebral Fusion Device With Bone Graft, Lumbar9
HAOInstrument, Surgical, Non-Powered7

GMDN & GCC registration

  • GMDN code 66306 · non‑implantable
  • Single‑use 0% · sterile 0% · Rx‑only 99% · 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

Height (Millimeter) · 9Angle (degree) · 7Length (Inch) · 5Width (Millimeter) · 4Length (Millimeter) · 4

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

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

473 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Neurosurgical curette, reusable", from 9 companies. The largest labeler is Boss Instruments, Ltd., Inc. with 78% of records.

Which FDA product codes apply?

HAO (INSTRUMENT, SURGICAL, NON-POWERED), GZX (INSTRUMENT, MICROSURGICAL), FZS (CURETTE, SURGICAL, GENERAL USE), LXH (Orthopedic Manual Surgical Instrument)

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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