Consulting Wallah › Device Explorer › Dental › Dental implant suprastructure reamer guide
Device Explorer · FDA GUDID · GMDN 63664

Dental implant suprastructure reamer guide

A manually-operated dental laboratory instrument intended to help guide a manual reamer during smoothing and refining of the surface of the screw channel, screw seat and implant/abutment connection of a dental implant suprastructure, to remove minor casting fl

US‑registered devices74in commercial distribution
Companies8labelers on GUDID
Single‑use4%of device records
Sterile0%labelled sterile
Prescription91%Rx‑only share
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Share of device records

Southern Implants (Pty) Ltd3851%
Implant Protesis Dental 2004 Sl2534%
Preat Corporation34%
Snucone Co.,Ltd.34%
Cowellmedi Co.,Ltd23%
Dentech Corporation11%
Jedmed Instrument Company11%
Thommen Medical Ag11%

Top labelers

CompanyDevicesShare
Southern Implants (Pty) Ltd3851%
Implant Protesis Dental 2004 Sl2534%
Preat Corporation34%
Snucone Co.,Ltd.34%
Cowellmedi Co.,Ltd23%
Dentech Corporation11%
Jedmed Instrument Company11%
Thommen Medical Ag11%

Company = labeler of record on GUDID. 8 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

N/ANADENTECHPreatJEDMEDGUIDE STENT TRIMMERDental InstrumentIPDGauge for reamer

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

FDA product codes

CodeNameDevices
NDPAccessories, Implant, Dental, Endosseous69
NDPAccessories, implant, dental, endosseous3
EJLBur, Dental1
GCXApparatus, Suction, Operating-Room, Wall Vacuum Powered1

GMDN & GCC registration

  • GMDN code 63664 · non‑implantable
  • Single‑use 4% · sterile 0% · Rx‑only 91% · 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 dental implant suprastructure reamer guide products are registered in the US?

74 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Dental implant suprastructure reamer guide", from 8 companies. The largest labeler is Southern Implants (Pty) Ltd with 51% of records.

Which FDA product codes apply?

NDP (Accessories, Implant, Dental, Endosseous), NDP (Accessories, implant, dental, endosseous), EJL (Bur, Dental), GCX (Apparatus, Suction, Operating-Room, Wall Vacuum Powered)

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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