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Device Explorer · FDA GUDID · GMDN 47974

Dental implant x-ray template

A non-sterile device intended to be used by a dentist or a surgeon to radiographically determine the appropriate size of a dental implant to be inserted into the jawbone of a patient prior to dental surgery. It is typically made of a translucent plastic sheet

US‑registered devices65in commercial distribution
Companies10labelers on GUDID
Single‑use12%of device records
Sterile0%labelled sterile
Prescription94%Rx‑only share
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Share of device records

Altatec Gmbh1828%
Nobel Biocare Ab1117%
Institut Straumann Ag812%
Adin Dental Implant Systems Ltd711%
Zimvie Us Corp Llc711%
Dentsply Implants Manufacturing Gmbh69%
Biohorizons Implant Systems, Inc46%
Etablissements Anthogyr23%

Top labelers

CompanyDevicesShare
Altatec Gmbh1828%
Nobel Biocare Ab1117%
Institut Straumann Ag812%
Adin Dental Implant Systems Ltd711%
Zimvie Us Corp Llc711%
Dentsply Implants Manufacturing Gmbh69%
Biohorizons Implant Systems, Inc46%
Etablissements Anthogyr23%
American Dental Implant Corporation12%
Thommen Medical Ag12%

Company = labeler of record on GUDID. 10 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

PrimeTaperDS OmniTaperANKYLOS®ASTRA TECH Implant System® EVASTRA TECH Implant System®Nobel Biocare N1™NobelActive®NobelParallel™NobelSpeedy®NobelReplace®Replace Select™Brånemark System®Radiographic Template Unp™Radiographic Template Touareg™ - S / OSRadiographic Template One™Radiographic Template Swell™

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

FDA product codes

CodeNameDevices
MQCMouthguard, prescription154
NDPAccessories, Implant, Dental, Endosseous33
NDPAccessories, implant, dental, endosseous32
KMYPOSITIONER, TOOTH, PREFORMED17
NXCAligner, sequential17
EBGCROWN AND BRIDGE, TEMPORARY, RESIN17

GMDN & GCC registration

  • GMDN code 47974 · non‑implantable
  • Single‑use 12% · sterile 0% · Rx‑only 94% · OTC 2%
  • 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 x-ray template products are registered in the US?

65 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Dental implant x-ray template", from 10 companies. The largest labeler is Altatec Gmbh with 28% of records.

Which FDA product codes apply?

MQC (Mouthguard, prescription), NDP (Accessories, Implant, Dental, Endosseous), NDP (Accessories, implant, dental, endosseous), KMY (POSITIONER, TOOTH, PREFORMED)

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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