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Device Explorer · FDA GUDID · GMDN 31335

Bone curette, reusable

A manual surgical instrument designed for cutting and excising bone tissue typically during an orthopaedic or a plastic surgery procedure. It is typically designed as a long, slender instrument with a handle at the proximal end and a concave, spoon-like tip wh

US‑registered devices15,771in commercial distribution
Companies189labelers on GUDID
Single‑use5%of device records
Sterile0%labelled sterile
Prescription63%Rx‑only share
ShareLinkedIn

Share of device records

Life Instrument Corporation1,65310%
Aspen Surgical Products, Inc.7155%
Novo Surgical, Inc.6714%
Integra Lifesciences Production Corporation6594%
Highridge Medical, Llc6464%
Surgical Direct, Inc.6104%
Avalign Technologies, Inc.5784%
Ambler Surgical Corp.5634%

Top labelers

CompanyDevicesShare
Life Instrument Corporation1,65310%
Aspen Surgical Products, Inc.7155%
Novo Surgical, Inc.6714%
Integra Lifesciences Production Corporation6594%
Highridge Medical, Llc6464%
Surgical Direct, Inc.6104%
Avalign Technologies, Inc.5784%
Ambler Surgical Corp.5634%
Medtronic Sofamor Danek, Inc.5393%
Alphatec Spine, Inc.4813%
Sklar Corporation4203%
Ortho-Med, Inc.3422%

Company = labeler of record on GUDID. 189 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

Posterior TLIFInstrumentXIA 3RELIANCE ALRELIANCEXIA 4.5RELIANCE LITeO.I.C. TITANIUMNASTILLE Bone CurettesCarboClear Cervical Cage / VBR SystemCarboClear Lumbar Cage SystemCharnley Bone Curette, T Handle, Small, 370mm O/Charnley Bone Curette, T Handle, Medium, 370mm OMuller Curette, Large, 240mm O/L, 27mm x 37mm CuMuller Curette, Small, 270mm O/L, 9mm x 13mm Cup

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

FDA product codes

CodeNameDevices
FZSCurette, Surgical, General Use3,791
HTFCURETTE2,966
FZSCURETTE, SURGICAL, GENERAL USE2,203
HAOINSTRUMENT, SURGICAL, NON-POWERED1,378
HTFCurette1,030
EMKCURETTE, SURGICAL, DENTAL622

GMDN & GCC registration

  • GMDN code 31335 · non‑implantable
  • Single‑use 5% · sterile 0% · Rx‑only 63% · 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) · 1,502Width (Millimeter) · 351Height (Millimeter) · 151Length (Centimeter) · 136Angle (degree) · 123Length (Millimeter) · 109

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

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

15,771 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Bone curette, reusable", from 189 companies. The largest labeler is Life Instrument Corporation with 10% of records.

Which FDA product codes apply?

FZS (Curette, Surgical, General Use), HTF (CURETTE), FZS (CURETTE, SURGICAL, GENERAL USE), HAO (INSTRUMENT, SURGICAL, NON-POWERED)

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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