PROTEXA ENDOVASCULAR

FDA Device Registration & Listing · Grand Junction, CO, US · Registration 3034619061

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
3034619061
FEI Number
3034619061
Entity Name
PROTEXA ENDOVASCULAR
City/State/Country
Grand Junction, CO, US
Establishment Address
1556 Wellington Avenue, Grand Junction, CO 81501, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Protexa Endovascular (Owner Number: 10092300)
Owner / Operator Contact Address
1556 Wellington Avenue, Grand Junction, CO 81501, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
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
QEW Peripheral Mechanical Thrombectomy With Aspiration Cardiovascular Class 2 870.5150 2024-12-20
QEX Coronary Mechanical Thrombectomy With Aspiration Cardiovascular Class 2 870.5150 2024-12-20

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Protexa Endovascular
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K241362 Surmodics,Inc. Pounce XL Thrombectomy System (PTS-1011-7F135) 2024-09-11
K220887 Inari Medical Mini-ClotTriever Thrombectomy System 2022-08-04
K250421 Inari Medical, Inc. InThrill™ Thrombectomy System 2025-05-12
K192036 Inari Medical ClotTriever Thrombectomy System 2019-08-29

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3017823876 Expanse Medical Inc. Pleasanton, CA, US
3015615738 Penumbra Inc. Salt Lake City, UT, US
3029444898 ICHOR VASCULAR INC Brecksville, OH, US
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3034619061. Last updated year: 2026. Please use registration number 3034619061 when referencing this establishment in official correspondence.
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