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Device Explorer · FDA GUDID · GMDN 37413

Orthodontic ligature director

A hand-held dental instrument used to tuck and direct ligatures under the archwire or bracket wings or to push archwires or auxiliaries into position. This is a reusable device.

US‑registered devices297in commercial distribution
Companies37labelers on GUDID
Single‑use3%of device records
Sterile2%labelled sterile
Prescription41%Rx‑only share
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Share of device records

Hu-Friedy Mfg. Co., Llc7024%
Nordent Manufacturing Inc4415%
Lm-Dental279%
Ortho Arch Company Inc248%
Ortho Organizers, Inc.165%
Leone Spa155%
Dental Morelli Ltda103%
J & J Instruments Inc93%

Top labelers

CompanyDevicesShare
Hu-Friedy Mfg. Co., Llc7024%
Nordent Manufacturing Inc4415%
Lm-Dental279%
Ortho Arch Company Inc248%
Ortho Organizers, Inc.165%
Leone Spa155%
Dental Morelli Ltda103%
J & J Instruments Inc93%
Ormco Corporation83%
3M Unitek Corporation72%
Forestadent Bernhard Förster Gmbh62%
Avalign Technologies, Inc.52%

Company = labeler of record on GUDID. 37 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

SPEED Torquing KeyDTCReusable Ligature CarrierN.A.LMDentalNAAESCULAPOrmcoBOSS InstrumentsORTHO ARCHORTH ARCHThe Orthodontic StoreKarl SchumacherA. Titan InstrumentsN/AOrthoquest

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

FDA product codes

CodeNameDevices
ECPINSTRUMENT, LIGATURE TUCKING, ORTHODONTIC90
ECPInstrument, Ligature Tucking, Orthodontic84
DZNINSTRUMENTS, DENTAL HAND44
DZNInstruments, Dental Hand41
JEXPLIER, ORTHODONTIC19
JEXPlier, Orthodontic12

GMDN & GCC registration

  • GMDN code 37413 · non‑implantable
  • Single‑use 3% · sterile 2% · Rx‑only 41% · 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 ligature director products are registered in the US?

297 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Orthodontic ligature director", from 37 companies. The largest labeler is Hu-Friedy Mfg. Co., Llc with 24% of records.

Which FDA product codes apply?

ECP (INSTRUMENT, LIGATURE TUCKING, ORTHODONTIC), ECP (Instrument, Ligature Tucking, Orthodontic), DZN (INSTRUMENTS, DENTAL HAND), DZN (Instruments, Dental Hand)

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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