R3 VASCULAR, INC.

FDA Device Registration & Listing · Mountain View, CA, US · Registration 3017991474

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
3017991474
FEI Number
3017991474
Entity Name
R3 VASCULAR, INC.
City/State/Country
Mountain View, CA, US
Establishment Address
1145 Terra Bella Ave., Suite A, Mountain View, CA 94043, US
Establishment Type(s)
Manufacture Device in the United States for Export Only
Owner / Operator
R3 Vascular, Inc. (Owner Number: 10081919)
Owner / Operator Contact Address
1145 Terra Bella Ave., Mountain View, CA 94043, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NIU Stent, Superficial Femoral Artery, Drug-Eluting Unknown Class 3 N/A 2021-05-26

Official Correspondent

Kristin Ellis

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

R3 Vascular, 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 3017991474. Last updated year: 2026. Please use registration number 3017991474 when referencing this establishment in official correspondence.
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