Nordson MEDICAL (CA), LLC

FDA Device Registration & Listing · Huntingtn Bch, CA, US · Registration 2032228

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
2032228
FEI Number
3003166981
Entity Name
Nordson MEDICAL (CA), LLC
City/State/Country
Huntingtn Bch, CA, US
Establishment Address
7612 Woodwind Drive, Huntingtn Bch, CA 92647, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Nordson MEDICAL (CA), LLC (Owner Number: 10027667)
Owner / Operator Contact Address
7612 Woodwind Drive, Huntington Beach, CA 92647, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Elite Vascular Access Kit

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass Cardiovascular Class 2 870.4210 2008-11-22
DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass Cardiovascular Class 2 870.4210 2013-01-02
DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass Cardiovascular Class 2 870.4210 2013-01-02
DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass Cardiovascular Class 2 870.4210 2013-01-02
DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass Cardiovascular Class 2 870.4210 2015-03-13
DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass Cardiovascular Class 2 870.4210 2015-03-18
DRE Dilator, Vessel, For Percutaneous Catheterization Cardiovascular Class 2 870.1310 2008-11-22

Official Correspondent

Ben Do

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Nordson MEDICAL (CA), LLC
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3005448067 Nordson MEDICAL Mexico Guaymas Sonora, MX

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K832124 Med-West, Inc. CPC, COUBLE LUMEN CARDIOPLEGIA-AIR ASPI 1983-08-12
K162500 Spyder Medical Ostial Sprit Cannulae 2017-01-12

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0003-2022 Medtronic Perfusion Systems 2
Medtronic Bio-Medicus Insertion Kits, Model number 96553, Pediatric Insertion Kit, Sterile; and Model number 96551, Venous Insertion Kit, Sterile.
Z-0021-2018 OriGen Biomedical, Inc. 2
The OriGen Reinforced Dual Lumen catheter (RDLC) is a duel lumen catheter with a wire reinforcement layer on the tip of the device. A thin sheath is used to cover and secure the wire layer and is heat shrunk into a permanent position.

Similar Registrations

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3009380063 Medtronic Distribution Center Memphis, TN, US
2916596 THORATEC CORP. PLEASANTON, CA, US
1836324 Rose Medical Grand Rapids, MI, US
3019807891 CENTERPIECE S. DE R.L DE C.V (sterilization site) Tijuana Baja California, MX
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2032228. Last updated year: 2026. Please use registration number 2032228 when referencing this establishment in official correspondence.
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