US Vascular

FDA Device Registration & Listing · Beaverton, OR, US · Registration 3010089756

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
3010089756
FEI Number
3010089756
Entity Name
US Vascular
City/State/Country
Beaverton, OR, US
Establishment Address
7874 SW Nimbus Avenue, Beaverton, OR 97008, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
US Vascular (Owner Number: 10045849)
Owner / Operator Contact Address
7874 SW Nimbus Avenue, Beaverton, OR 97008, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K131860
PMA Number
N/A

All Registered Proprietary Names

VascuLab 4043 VascuLab 4040 VascuLab 4040 GSX

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
JOP Transducer, Ultrasonic Cardiovascular Class 2 870.2880 2014-01-06

Official Correspondent

Galen Spooner

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

US Vascular
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 3010089756. Last updated year: 2026. Please use registration number 3010089756 when referencing this establishment in official correspondence.
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