Device Explorer · FDA GUDID · GMDN 47997

Bone grafting cannula

A rigid tube intended to be used surgically to introduce a bone void filler (e.g., a bone matrix implant/bone substitute) in voids or gaps of the skeletal system (i.e., extremities, craniofacial bone, spine, and pelvis) to fill defects in the bone structure cr

US‑registered devices94in commercial distribution
Companies19labelers on GUDID
Single‑use81%of device records
Sterile81%labelled sterile
Prescription100%Rx‑only share
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Share of device records

Beijing Allgens Medical Science & Technology Co., Ltd.1516%
Synthes Gmbh1314%
Zimmer Knee Creations, Inc.1011%
Shanghai Kinetic Medical Co., Ltd.910%
Medos International Sàrl910%
Biomet Orthopedics, Llc89%
Seaspine Orthopedics Corporation66%
Stryker Corporation44%

Top labelers

CompanyDevicesShare
Beijing Allgens Medical Science & Technology Co., Ltd.1516%
Synthes Gmbh1314%
Zimmer Knee Creations, Inc.1011%
Shanghai Kinetic Medical Co., Ltd.910%
Medos International Sàrl910%
Biomet Orthopedics, Llc89%
Seaspine Orthopedics Corporation66%
Stryker Corporation44%
Biomet Spine Llc44%
Ace Surgical Supply Co., Inc.44%
Joline Gmbh & Co. Kg22%
Zimmer, Inc.22%

Company = labeler of record on GUDID. 19 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

HydroSet XTBongold Bone Graft MaterialBone Biopsy DeviceOne-ShotBone Filler DeviceFiller Kit FlexFiller KitAccuPort® CannulaPrecision Cannula11 GA x 200mm End Hip AccuPortAcuPort Zone Cannulated 8 GA x 200mmAccuPort Multi Cannulated 8 GA x 200mmAccuPort End Cannulated 8 GA x 200mmAccuPort Side Delivery Cannula 11 Ga x 120mmInFix® Anterior Lumbar SystemAccuPort Multi Directional Delivery Canula 8 Ga

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

FDA product codes

CodeNameDevices
MQVFiller, Bone Void, Calcium Compound21
FMFSyringe, Piston14
GAANEEDLE, ASPIRATION AND INJECTION, DISPOSABLE13
FGYCannula, Injection12
HRXArthroscope8
MQVFILLER, BONE VOID, CALCIUM COMPOUND7

GMDN & GCC registration

  • GMDN code 47997 · non‑implantable
  • Single‑use 81% · sterile 81% · Rx‑only 100% · 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 (Millimeter) · 16Needle Gauge (Gauge) · 14Outer Diameter (Millimeter) · 7

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

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

94 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Bone grafting cannula", from 19 companies. The largest labeler is Beijing Allgens Medical Science & Technology Co., Ltd. with 16% of records.

Which FDA product codes apply?

MQV (Filler, Bone Void, Calcium Compound), FMF (Syringe, Piston), GAA (NEEDLE, ASPIRATION AND INJECTION, DISPOSABLE), FGY (Cannula, Injection)

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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