Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3012276280

FEI Number

3012276280

Entity Name

KA Medical

City/State/Country

Arden Hills, MN, US

Establishment Address

1265 Grey Fox Road, Suite 550, Arden Hills, MN 55112, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Merit Medical Systems, Inc. (Owner Number: 1721504)

Owner / Operator Contact Address

1600 West Merit Parkway, --, South Jordan, UT 84095, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K182944

PMA Number

N/A

All Registered Proprietary Names

Siege Vascular Plug Micro Plug Set

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KRD	Device, Vascular, For Promoting Embolization	Cardiovascular	Class 2	870.3300	2024-05-06
KRD	Device, Vascular, For Promoting Embolization	Cardiovascular	Class 2	870.3300	2020-12-14

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Merit Medical Systems, 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
3021179744	VIEW POINT MEDICAL, INC.	Carlsbad, CA, US
2032338	Merit Medical Systems, Inc.	ALISO VIEJO, CA, US
1125782	MERIT MEDICAL SYSTEMS, INC	Chester, VA, US
9615728	BIOSPHERE MEDICAL, S.A.	Roissy Val-d'Oise, FR
3010665433	Merit Medical Systems, Inc.	Houston, TX, US

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0002-2017	Merit Medical Systems, Inc.	2	Merit Inflation Syringe Kit. Catalog Number KOS-02857
Z-0026-2020	Merit Medical Systems, Inc.	2	Custom Procedure Kit, Custom Kit, REF/Product Code: K12T-03688, single use, RX Only, Sterile EO, LATEX FREE, UDI: (01)00884450389409
Z-0027-2020	Merit Medical Systems, Inc.	2	Custom Procedure Kit, Vein Kit, Product Code/REF: K12T-10167, single use, RX Only, Sterile EO, UDI: (01) 00884450390580

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2134812	VASCULAR SOLUTIONS LLC	Maple Grove, MN, US
2029275	Sterigenics U.S., LLC	Corona, CA, US
3008853977	Stryker Neurovascular	Fremont, CA, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3012276280. Last updated year: 2026. Please use registration number 3012276280 when referencing this establishment in official correspondence.