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Device Explorer · FDA GUDID · GMDN 47866

Orthopaedic implant/instrument dismantling device

A device designed to dismantle (take apart) the component parts of an implant or a surgical instrument that have previously been assembled. It may be used as a stand-alone device or in combination with another device to control the dismantling process of, e.g.

US‑registered devices195in commercial distribution
Companies26labelers on GUDID
Single‑use1%of device records
Sterile0%labelled sterile
Prescription83%Rx‑only share
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Share of device records

Nuvasive, Inc.5428%
Biomet Orthopedics, Llc2613%
Depuy (Ireland)2513%
Ldr Spine Usa, Inc.158%
Cg Medtech Co.,Ltd.137%
Wright Medical Technology, Inc.105%
Depuy Orthopaedics, Inc.74%
Limacorporate Spa74%

Top labelers

CompanyDevicesShare
Nuvasive, Inc.5428%
Biomet Orthopedics, Llc2613%
Depuy (Ireland)2513%
Ldr Spine Usa, Inc.158%
Cg Medtech Co.,Ltd.137%
Wright Medical Technology, Inc.105%
Depuy Orthopaedics, Inc.74%
Limacorporate Spa74%
Tornier, Inc.63%
Exactech, Inc.53%
Xtant Medical Holdings, Inc.32%
Wenzel Spine, Inc.32%

Company = labeler of record on GUDID. 26 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

Extraction ToolUnity Total Knee SystemBiMobile Dual Mobility System - InstrumentsLINK Instruments - Impactors, extractors and insTornier FlexIMPULSIONROI-AGeneral instrumentationVerteFITAvenue TNASIDEKICKCANCELLO-PUREOSS™ReLineTLX

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 INSTRUMENT100
LXHOrthopedic manual surgical instrument26
LXHOrthopedic Manual Surgical Instrument22
HWBEXTRACTOR17
HXCWRENCH5
JWHPROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEM3

GMDN & GCC registration

  • GMDN code 47866 · non‑implantable
  • Single‑use 1% · sterile 0% · Rx‑only 83% · OTC 1%
  • UAE: MOHAP / DoH medical device registration and an authorised representative are required; Saudi: SFDA MDMA. We check status on request.

Size attributes recorded

No structured size data on the register.

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

How many orthopaedic implant/instrument dismantling device products are registered in the US?

195 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Orthopaedic implant/instrument dismantling device", from 26 companies. The largest labeler is Nuvasive, Inc. with 28% of records.

Which FDA product codes apply?

LXH (ORTHOPEDIC MANUAL SURGICAL INSTRUMENT), LXH (Orthopedic manual surgical instrument), LXH (Orthopedic Manual Surgical Instrument), HWB (EXTRACTOR)

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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