POLARISAR INC

FDA Device Registration & Listing · Richardson, TX, US · Registration 3025287527

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
3025287527
FEI Number
3025287527
Entity Name
POLARISAR INC
City/State/Country
Richardson, TX, US
Establishment Address
2221 Lakeside Blvd Ste 1125, Richardson, TX 75082, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
PolarisAR Inc. (Owner Number: 10090108)
Owner / Operator Contact Address
2221 Lakeside BLVD Ste 1125, Richardson, TX 75082, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K232176
PMA Number
N/A

All Registered Proprietary Names

STELLAR Knee

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
SBF Orthopedic Augmented Reality Neurology Class 2 882.4560 2024-02-15

Official Correspondent

Brandon Keirns

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

PolarisAR Inc.
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3025287527. Last updated year: 2026. Please use registration number 3025287527 when referencing this establishment in official correspondence.
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