Consulting Wallah › Device Explorer › Other devices › Orthodontic wire
Device Explorer · FDA GUDID · GMDN 16204

Orthodontic wire

A thread or slender rod of metal (e.g., stainless steel, precious metal) incorporated into an orthodontic appliance, typically as part of an orthodontic appliance system. It is available in various dimensions and grades, and is used to exert pressure on teeth

US‑registered devices8,229in commercial distribution
Companies34labelers on GUDID
Single‑use99%of device records
Sterile0%labelled sterile
Prescription46%Rx‑only share
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Share of device records

American Orthodontics Corporation2,16026%
Pg Supply, Inc.1,99724%
Reliance Orthodontic Products Inc1,36017%
Aditek Do Brasil S/A88611%
Tp Orthodontics Inc5877%
Dentaurum Gmbh & Co.Kg2063%
Orthosource1372%
Leone Spa1372%

Top labelers

CompanyDevicesShare
American Orthodontics Corporation2,16026%
Pg Supply, Inc.1,99724%
Reliance Orthodontic Products Inc1,36017%
Aditek Do Brasil S/A88611%
Tp Orthodontics Inc5877%
Dentaurum Gmbh & Co.Kg2063%
Orthosource1372%
Leone Spa1372%
Scheu-Dental Gmbh1141%
Ortho Arch Company Inc951%
Rmo, Inc.861%
Forestadent Bernhard Förster Gmbh821%

Company = labeler of record on GUDID. 34 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

DTCNiTi SuperElastic Wire, Euro II, .021x.025, LoweNiTi SuperElastic Wire, Euro II, .021x.025, UppeNiTi SuperElastic Wire, Euro II, .019x.025, LoweNiTi SuperElastic Wire, Euro II, .019x.025, UppeNiTi SuperElastic Wire, Euro II, .018x.025, LoweNiTi SuperElastic Wire, Euro II, .018x.025, UppeNiTi SuperElastic Wire, Euro II, .018x.022, LoweNiTi SuperElastic Wire, Euro II, .018x.022, UppeNiTi SuperElastic Wire, Euro II, .017x.025, LoweNiTi SuperElastic Wire, Euro II, .017x.025, UppeNiTi SuperElastic Wire, Euro II, .017x.022, LoweNiTi SuperElastic Wire, Euro II, .017x.022, UppeNiTi SuperElastic Wire, Euro II, .016x.022, LoweNiTi SuperElastic Wire, Euro II, .016x.022, UppeNiTi SuperElastic Wire, Euro II, .016x.016, Lowe

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

FDA product codes

CodeNameDevices
DZCWIRE, ORTHODONTIC6,230
DZCWire, Orthodontic3,405
EHPClasp, Preformed147
ECOSPRING, ORTHODONTIC64
EHPCLASP, PREFORMED52
EJFBRACKET, METAL, ORTHODONTIC39

GMDN & GCC registration

  • GMDN code 16204 · non‑implantable
  • Single‑use 99% · sterile 0% · Rx‑only 46% · 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 orthodontic wire products are registered in the US?

8,229 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Orthodontic wire", from 34 companies. The largest labeler is American Orthodontics Corporation with 26% of records.

Which FDA product codes apply?

DZC (WIRE, ORTHODONTIC), DZC (Wire, Orthodontic), EHP (Clasp, Preformed), ECO (SPRING, ORTHODONTIC)

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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