CERUS ENDOVASCULAR, INC.

FDA Device Registration & Listing · Fremont, CA, US · Registration 3013408612

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
3013408612
FEI Number
3013408612
Entity Name
CERUS ENDOVASCULAR, INC.
City/State/Country
Fremont, CA, US
Establishment Address
47757 Fremont Boulevard, Fremont, CA 94538, US
Establishment Type(s)
Manufacture Device in the United States for Export Only
Owner / Operator
Cerus Endovascular, Inc. (Owner Number: 10076754)
Owner / Operator Contact Address
47757 Fremont Boulevard, Fremont, CA 94538, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Neqstent Contour Neurovascular System

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
OPR Intrasaccular Flow Disruption Device Unknown Class 3 N/A 2025-01-06

Official Correspondent

Brittany Lowe

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Cerus Endovascular, 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 3013408612. Last updated year: 2026. Please use registration number 3013408612 when referencing this establishment in official correspondence.
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