Consulting Wallah › Device Explorer › Other devices › Bone graft funnel
Device Explorer · FDA GUDID · GMDN 47872

Bone graft funnel

A device designed to deliver bone graft filling material (autologous, allogeneic, xenogeneic, or synthetic) during an orthopaedic procedure to enable the filling of bone gaps intended to be fused. It is a funnel-shaped device; the funnel being bowl-shaped with

US‑registered devices475in commercial distribution
Companies53labelers on GUDID
Single‑use4%of device records
Sterile1%labelled sterile
Prescription84%Rx‑only share
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Share of device records

Medtronic Sofamor Danek, Inc.15833%
Alphatec Spine, Inc.4710%
Depuy Spine, Llc296%
Highridge Medical, Llc204%
Osstem Implant Co., Ltd.194%
Seaspine Orthopedics Corporation184%
W.H. Holden, Inc.153%
Integrity Implants Inc.153%

Top labelers

CompanyDevicesShare
Medtronic Sofamor Danek, Inc.15833%
Alphatec Spine, Inc.4710%
Depuy Spine, Llc296%
Highridge Medical, Llc204%
Osstem Implant Co., Ltd.194%
Seaspine Orthopedics Corporation184%
W.H. Holden, Inc.153%
Integrity Implants Inc.153%
Wheelhouse Medical123%
Synthes Gmbh92%
Axis Spine Technologies Ltd71%
A. Titan Instruments, Inc.71%

Company = labeler of record on GUDID. 53 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

CarboClear Lumbar Cage SystemAxis Spine Technologies ALIF System InstrumentKOHDENTVERTEBRISHarmony Posterior InstrumentsDisc Preparation InstrumentsFlareHawkToro-LROI-TBreckenridge ACDF SystemMETRx® SystemMedtronic Reusable InstrumentsnaWheelhouse Medical SpecialsFUNNEL PACKER 3.0mm STR D/EFUNNEL - STAINLESS 3ml SYRINGE

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

FDA product codes

CodeNameDevices
LXHOrthopedic manual surgical instrument225
LXHORTHOPEDIC MANUAL SURGICAL INSTRUMENT80
LXHOrthopedic Manual Surgical Instrument77
NDPAccessories, Implant, Dental, Endosseous22
NBHAccessories, arthroscopic21
DZNINSTRUMENTS, DENTAL HAND14

GMDN & GCC registration

  • GMDN code 47872 · non‑implantable
  • Single‑use 4% · sterile 1% · Rx‑only 84% · 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

Lumen/Inner Diameter (Millimeter) · 1Outer Diameter (Millimeter) · 1Length (Millimeter) · 1Total Volume (Milliliter) · 1Angle (degree) · 1

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

How many bone graft funnel products are registered in the US?

475 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Bone graft funnel", from 53 companies. The largest labeler is Medtronic Sofamor Danek, Inc. with 33% of records.

Which FDA product codes apply?

LXH (Orthopedic manual surgical instrument), LXH (ORTHOPEDIC MANUAL SURGICAL INSTRUMENT), LXH (Orthopedic Manual Surgical Instrument), NDP (Accessories, Implant, Dental, Endosseous)

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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