CATHX MEDICAL INC

FDA Device Registration & Listing · Arden Hills, MN, US · Registration 3027226463

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
3027226463
FEI Number
3027226463
Entity Name
CATHX MEDICAL INC
City/State/Country
Arden Hills, MN, US
Establishment Address
1275 Red Fox Rd, Arden Hills, MN 55112, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
CathX Medical Inc (Owner Number: 10077166)
Owner / Operator Contact Address
235 Charcot Avenue, San Jose, CA 95131, 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
QEW Peripheral Mechanical Thrombectomy With Aspiration Cardiovascular Class 2 870.5150 2025-08-29

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

CathX Medical Inc
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3016704395 CATHX MEDICAL INC San Jose, CA, US

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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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3027226463. Last updated year: 2026. Please use registration number 3027226463 when referencing this establishment in official correspondence.
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