STOMATOTECH

FDA Device Registration & Listing · Pierrefonds Quebec, CA · Registration 3010966817

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3010966817
FEI Number
3010966817
Entity Name
STOMATOTECH
City/State/Country
Pierrefonds Quebec, CA
Establishment Address
4919 Boul St Charles, Pierrefonds Quebec H9H 3E4, CA
Establishment Type(s)
Export Device to the United States But Perform No Other Operation on Device,Develop Specifications But Do Not Manufacture At This Facility,Manufacture Medical Device
Owner / Operator
Stomatotech (Owner Number: 10046960)
Owner / Operator Contact Address
4919 Boul Saints Charles, Pierrefonds, CA-QC QC H9H 3E4, CA
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Crown Down Drilling Kit

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
QRQ Non-Irrigation Endosseous Dental Implant Drill Bits Dental Class 1 872.3980 2025-11-17

Official Correspondent

No official correspondent registered.

US Agent Details

David Lennarz Business: Registrar corp Email: david.lennarz@registrarcorp.com Phone: (757) 2240177

Related Public Records

Same Entity

Stomatotech
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010966817. Last updated year: 2026. Please use registration number 3010966817 when referencing this establishment in official correspondence.
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