Device Explorer · FDA GUDID · GMDN 60478

Bone access cannula

A sterile, sharp, hollow tubular metal instrument designed for percutaneous insertion to provide access to any bone of the body for a bone biopsy needle or guidewire, or for a bone marrow aspiration technique, or for inserting therapeutic materials, including

US‑registered devices411in commercial distribution
Companies36labelers on GUDID
Single‑use93%of device records
Sterile91%labelled sterile
Prescription89%Rx‑only share
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Share of device records

Ranfac Corp.14235%
Arthrex, Inc.4812%
Medtronic Sofamor Danek, Inc.379%
Stryker Corporation215%
Lacey Manufacturing Company, Llc154%
Izi Medical Products, Llc143%
Medos International Sàrl143%
Surgentec, Llc123%

Top labelers

CompanyDevicesShare
Ranfac Corp.14235%
Arthrex, Inc.4812%
Medtronic Sofamor Danek, Inc.379%
Stryker Corporation215%
Lacey Manufacturing Company, Llc154%
Izi Medical Products, Llc143%
Medos International Sàrl143%
Surgentec, Llc123%
Tecres Spa123%
Alphatec Spine, Inc.102%
Benvenue Medical, Inc.92%
Joline Gmbh & Co. Kg61%

Company = labeler of record on GUDID. 36 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

IVASLITeiVASXIA PRECISION SYSTEMNADilatorCannulaBone DrillsPuncture NeedlesAVS ARIASpeedTrack Short Tip Introducer Cannula & StyletRapidIntro Bevel Tip Introducer Cannula & StyletVertebra Introducer Working CannulaVertebra Introducer Device Introducer Cannula & Vertebra Access Device wth Trocar Tip Access NeeAccess Kit

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

FDA product codes

CodeNameDevices
KNWInstrument, Biopsy141
NBHAccessories, arthroscopic41
PDQNeurosurgical Nerve Locator27
GAANEEDLE, ASPIRATION AND INJECTION, DISPOSABLE27
LXHORTHOPEDIC MANUAL SURGICAL INSTRUMENT24
OARInjector, vertebroplasty (does not contain cement)20

GMDN & GCC registration

  • GMDN code 60478 · non‑implantable
  • Single‑use 93% · sterile 91% · Rx‑only 89% · 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

Needle Gauge (Gauge) · 175Length (Centimeter) · 107Length (Inch) · 51Length (Millimeter) · 28Outer Diameter (Millimeter) · 4

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

How many bone access cannula products are registered in the US?

411 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Bone access cannula", from 36 companies. The largest labeler is Ranfac Corp. with 35% of records.

Which FDA product codes apply?

KNW (Instrument, Biopsy), NBH (Accessories, arthroscopic), PDQ (Neurosurgical Nerve Locator), GAA (NEEDLE, ASPIRATION AND INJECTION, DISPOSABLE)

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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