Consulting Wallah › Device Explorer › Other devices › Bone graft packing block
Device Explorer · FDA GUDID · GMDN 47743

Bone graft packing block

A device designed to tightly compact (pack) an implant with a bone graft material (e.g., autologous, allogeneic, xenogeneic, or of synthetic origin) prior to the implantation of the implant. It is typically a small, box-shaped device consisting of two parts, a

US‑registered devices217in commercial distribution
Companies34labelers on GUDID
Single‑use11%of device records
Sterile0%labelled sterile
Prescription78%Rx‑only share
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Share of device records

Seaspine Orthopedics Corporation3617%
Medtronic Sofamor Danek, Inc.3114%
Spineart Sa2110%
Zoll-Dental209%
Silony Medical Gmbh94%
Synthes Gmbh94%
Curiteva, Inc.84%
Depuy Spine, Llc84%

Top labelers

CompanyDevicesShare
Seaspine Orthopedics Corporation3617%
Medtronic Sofamor Danek, Inc.3114%
Spineart Sa2110%
Zoll-Dental209%
Silony Medical Gmbh94%
Synthes Gmbh94%
Curiteva, Inc.84%
Depuy Spine, Llc84%
Vb Spine Llc73%
Cg Medtech Co.,Ltd.73%
Stryker Corporation63%
Highridge Medical, Llc63%

Company = labeler of record on GUDID. 34 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

ARIAAVS NAVIGATORAVSLoading BlockBreckenridge ACDF SystemTimberline Lateral Fusion SystemZyston Interbody Spacer SystemOmnia Medical PsiFOmnia Medical VBRBrickyard ALIFIndyImola-SilverstoneLatitude-C Cervical Interbody Spacer SystemImpulse Interbody Spacer SystemCEZANNE II Interbody Fusion SystemCEZANNE Lumbar Interbody Fusion Cage System

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 INSTRUMENT86
LXHOrthopedic manual surgical instrument57
LXHOrthopedic Manual Surgical Instrument22
MDMINSTRUMENT, MANUAL, SURGICAL, GENERAL USE20
MAXIntervertebral Fusion Device With Bone Graft, Lumbar17
ODPIntervertebral Fusion Device With Bone Graft, Cervical8

GMDN & GCC registration

  • GMDN code 47743 · non‑implantable
  • Single‑use 11% · sterile 0% · Rx‑only 78% · 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) · 3Height (Inch) · 2Width (Inch) · 2Length (Inch) · 2

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

How many bone graft packing block products are registered in the US?

217 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Bone graft packing block", from 34 companies. The largest labeler is Seaspine Orthopedics Corporation with 17% of records.

Which FDA product codes apply?

LXH (ORTHOPEDIC MANUAL SURGICAL INSTRUMENT), LXH (Orthopedic manual surgical instrument), LXH (Orthopedic Manual Surgical Instrument), MDM (INSTRUMENT, MANUAL, SURGICAL, GENERAL USE)

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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