Device Explorer · FDA GUDID · GMDN 47788

Spiral blade

An implantable, rod-like, cannulated device with spiralled flutes at the distal end and a smooth cylindrical portion at the proximal end that is used in combination with a bone fixation plate or an intramedullary nail to support bone fragments after fractures,

US‑registered devices219in commercial distribution
Companies1labelers on GUDID
Single‑use100%of device records
Sterile55%labelled sterile
Prescription100%Rx‑only share
ImplantableYesGMDN flag
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Share of device records

Synthes Gmbh219100%

Top labelers

CompanyDevicesShare
Synthes Gmbh219100%

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

Brand names on the register (sample)

NADHHSTFN-ADVANCEEXPert Nail

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 ACCESSORIES192
KTTAPPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE 80
HWCScrew, fixation, bone45
JDODEVICE, FIXATION, PROXIMAL FEMORAL, IMPLANT28
JDSNAIL, FIXATION, BONE22

GMDN & GCC registration

  • GMDN code 47788 · implantable
  • Single‑use 100% · sterile 55% · 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 spiral blade 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 "Spiral blade", from 1 companies. The largest labeler is Synthes Gmbh with 100% of records.

Which FDA product codes apply?

HSB (ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES), KTT (APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE ), HWC (Screw, fixation, bone), JDO (DEVICE, FIXATION, PROXIMAL FEMORAL, IMPLANT)

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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