Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3040314808

FEI Number

3040314808

Entity Name

NIKKISO CO., LTD. KANAZAWA PLANT

City/State/Country

Kanazawa-Shi, Ishikawa, JP

Establishment Address

3-1, Hokuyohdai, Kanazawa-Shi, Ishikawa 920-0177, JP

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

NIKKISO CO., LTD. (Owner Number: 8031561)

Owner / Operator Contact Address

20-3 EBISU 4-CHOME,, SHIBUYA-KU, JP-13 150-6022, JP

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K242155

PMA Number

N/A

All Registered Proprietary Names

DIALYSATE FILTERS DBB-06 PRO Hemodialysis Delivery System (DBB-06 PRO)

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KDI	Dialyzer, High Permeability With Or Without Sealed Dialysate System	Gastroenterology, Urology	Class 2	876.5860	2025-08-01

Official Correspondent

Satoko Hina

US Agent Details

Deno Zachary Business: MIC International Email: dzachary@micinternational.com Phone: (917) 3315789

Related Public Records

Same Entity

NIKKISO CO., LTD.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Other Registrations for Same Entity

Registration Number	Establishment Name	Location
8031561	NIKKISO CO., LTD. - SHIZUOKA PLANT	SHIZUOKA-KEN, JP
3014638255	NIKKISO CO., LTD.	SHIBUYA-KU Tokyo, JP
3027859369	M.E.Nikkiso Vietnam Co., Ltd.	Quang Ngai, VN
3008229990	M. E. NIKKISO CO., LTD.	Bangnumpeo, Chachoengsao, TH

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K811830	Cordis Corp.	C-DAK DUO-FLUX ARTIFICIAL KIDNEY	1981-09-21
K070320	Edwards Lifesciences Services GmbH	EDWARDS AQUARIUS HEMOFILTRATION SYSTEM, MODEL ABM 01	2007-06-07
K150880	Outset Medical	Tablo Console with Wireless Capability	2015-05-01

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0019-2025	Outset Medical, Inc.	2	Tablo Console, REF: PN-0003000, PN-0006000, part of the Tablo Hemodialysis System. The Tablo Hemodialysis System is indicated for use in patients with acute and/or chronic renal failure, with or without ultrafiltration, in an acute or chronic care facility.
Z-0028-2024	Fresenius Medical Care Holdings, Inc.	2	2008T Hemodialysis SYS, with CDX
Z-0029-2024	Fresenius Medical Care Holdings, Inc.	2	2008T Hemodialysis System without CDX
Z-0030-2024	Fresenius Medical Care Holdings, Inc.	2	2008T Hemodialysis System w/Bibag
Z-0031-2024	Fresenius Medical Care Holdings, Inc.	2	2008T GEN 2 Bibag without CDX

Similar Registrations

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3015349756	DIALITY, INC.	Irvine, CA, US
9611824	FRESENIUS MEDICAL CARE DEUTSCHLAND GMBH	SCHWEINFURT Bavaria, DE
3012149633	LIDER	MONTREVEL EN BRESSE Auvergne-Rhone-Alpes, FR
3005695808	SARMED SRL	IGLESIAS Sardegna, IT
3007137787	Nuwellis, Inc.	Eden Prairie, MN, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3040314808. Last updated year: 2026. Please use registration number 3040314808 when referencing this establishment in official correspondence.