BRIUS Technologies Inc.

FDA Device Registration & Listing · Carrollton, TX, US · Registration 3014680924

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
3014680924
FEI Number
3014680924
Entity Name
BRIUS Technologies Inc.
City/State/Country
Carrollton, TX, US
Establishment Address
2611 Westgrove Drive, Carrollton, TX 75006, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Brius (Owner Number: 10057851)
Owner / Operator Contact Address
2611 Westgrove Drive, #109, Carrollton, TX 75006, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K202792
PMA Number
N/A

All Registered Proprietary Names

Brius Software BRIUS Aligner

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
PNN Orthodontic Software Dental Class 2 872.5470 2020-10-26
NXC Aligner, Sequential Dental Class 2 872.5470 2021-12-27

Official Correspondent

Michael Lopez

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Brius
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 3014680924. Last updated year: 2026. Please use registration number 3014680924 when referencing this establishment in official correspondence.
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