Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3014397047

FEI Number

3014397047

Entity Name

RadiusXR Inc.

City/State/Country

Pleasanton, CA, US

Establishment Address

5994 W LAS POSITAS BLVD STE 101, Pleasanton, CA 94588, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility,Repack or Relabel Medical Device,Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device

Owner / Operator

RadiusXR, Inc. (Owner Number: 10049603)

Owner / Operator Contact Address

5994 W. Las Positas Blvd, Suite 101, Pleasanton, CA 94588, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Radius

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HPT	Perimeter, Automatic, Ac-Powered	Ophthalmic	Class 1	886.1605	2020-12-31

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

RadiusXR, Inc.

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 3014397047. Last updated year: 2026. Please use registration number 3014397047 when referencing this establishment in official correspondence.