Consulting Wallah › Device Explorer › Other devices › Bone nail trial, single-use
Device Explorer · FDA GUDID · GMDN 66957

Bone nail trial, single-use

A copy of a final orthopaedic bone nail designed to be introduced into the bone (e.g., proximal and/or distal end of the intramedullary canal of a long bone) to function as a reference for the subsequent introduction of the final bone nail, and typically also

US‑registered devices219in commercial distribution
Companies2labelers on GUDID
Single‑use100%of device records
Sterile99%labelled sterile
Prescription100%Rx‑only share
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Share of device records

Orthofix Srl21699%
Newclip Technics31%

Top labelers

CompanyDevicesShare
Orthofix Srl21699%
Newclip Technics31%

Company = labeler of record on GUDID. 2 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

Xpert HandXpert KneeORTHOFIX

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

FDA product codes

CodeNameDevices
HSBRod, Fixation, Intramedullary And Accessories216
HWCScrew, Fixation, Bone3

GMDN & GCC registration

  • GMDN code 66957 · non‑implantable
  • Single‑use 100% · sterile 99% · 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) · 216Outer Diameter (Millimeter) · 215

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

How many bone nail trial, single-use products are registered in the US?

219 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Bone nail trial, single-use", from 2 companies. The largest labeler is Orthofix Srl with 99% of records.

Which FDA product codes apply?

HSB (Rod, Fixation, Intramedullary And Accessories), HWC (Screw, Fixation, Bone)

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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