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Device Explorer · FDA GUDID · GMDN 56649

Tendon/ligament graft preparation station

An assembly of devices designed to provide the operator with a workstation for the preparation and pretensioning of a ligament and/or tendon graft prior to implantation. It typically consists of a work base to provide a stable platform on which the graft can b

US‑registered devices112in commercial distribution
Companies15labelers on GUDID
Single‑use0%of device records
Sterile0%labelled sterile
Prescription100%Rx‑only share
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Share of device records

Arthrex, Inc.5146%
Ldr Spine Usa, Inc.1412%
Conmed Corporation1110%
Medos International Sàrl98%
Stryker Corporation76%
Parcus Medical Llc65%
Biomet Orthopedics, Llc54%
Medicon Eg. Chirurgiemechaniker-Genossenschaft22%

Top labelers

CompanyDevicesShare
Arthrex, Inc.5146%
Ldr Spine Usa, Inc.1412%
Conmed Corporation1110%
Medos International Sàrl98%
Stryker Corporation76%
Parcus Medical Llc65%
Biomet Orthopedics, Llc54%
Medicon Eg. Chirurgiemechaniker-Genossenschaft22%
Karl Storz Gmbh & Co. Kg11%
S.B.M11%
Smith & Nephew, Inc.11%
Zimmer, Inc.11%

Company = labeler of record on GUDID. 15 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

NAn.a.MediconGraftTechMC+ROI-CROI-AROIROI-TAvenue LGeneral instrumentationAvenue TDistal Bicep Repair Socket Size GuideArthrex®Graft Sizing BlockGraft Preparation Board

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 INSTRUMENT70
LXHOrthopedic Manual Surgical Instrument12
HWTTEMPLATE9
MDMINSTRUMENT, MANUAL, SURGICAL, GENERAL USE8
NBHAccessories, arthroscopic6
NKBThoracolumbosacral Pedicle Screw System5

GMDN & GCC registration

  • GMDN code 56649 · non‑implantable
  • Single‑use 0% · sterile 0% · 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

No structured size data on the register.

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

How many tendon/ligament graft preparation station products are registered in the US?

112 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Tendon/ligament graft preparation station", from 15 companies. The largest labeler is Arthrex, Inc. with 46% of records.

Which FDA product codes apply?

LXH (ORTHOPEDIC MANUAL SURGICAL INSTRUMENT), LXH (Orthopedic Manual Surgical Instrument), HWT (TEMPLATE), 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.

How do I get quotes?

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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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