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Device Explorer · FDA GUDID · GMDN 63367

Long bone distraction intramedullary nail, magnetic

An implantable device in the form of a rigid rod, capable of adjusting in length, designed to be inserted into the medullary cavity of a long bone to hold the ends of a fractured bone in position to promote healing, or to support the bone in the presence of a

US‑registered devices446in commercial distribution
Companies1labelers on GUDID
Single‑use100%of device records
Sterile98%labelled sterile
Prescription100%Rx‑only share
ImplantableYesGMDN flag
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Share of device records

Nuvasive Specialized Orthopedics, Inc.446100%

Top labelers

CompanyDevicesShare
Nuvasive Specialized Orthopedics, Inc.446100%

Company = labeler of record on GUDID. 1 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

PRECICE® Bone Transport SystemPRECICE® STRYDE SystemPRECICE® SystemPRECICE® UNYTE Trauma Nail SystemPrecicePRECICE® Intramedullary Limb Lengthening SystemPRECICE® Trauma Nail System

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 Accessories469

GMDN & GCC registration

  • GMDN code 63367 · implantable
  • Single‑use 100% · sterile 98% · 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

Outer Diameter (Millimeter) · 157

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

How many long bone distraction intramedullary nail, magnetic products are registered in the US?

446 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Long bone distraction intramedullary nail, magnetic", from 1 companies. The largest labeler is Nuvasive Specialized Orthopedics, Inc. with 100% of records.

Which FDA product codes apply?

HSB (Rod, Fixation, Intramedullary And Accessories)

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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