Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3007635982

FEI Number

3007635982

Entity Name

Confluent Medical Technologies, Inc

City/State/Country

Fremont, CA, US

Establishment Address

47533 Westinghouse Dr, Fremont, CA 94539, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

Confluent Medical Technologies, Inc. (Owner Number: 10033958)

Owner / Operator Contact Address

6263 N. Scottsdale Road, Suite 224, Scottsdale, AZ 85250, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K011905

PMA Number

N/A

All Registered Proprietary Names

Aquatrack Hydrophilic Nitinol Guidewire

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
DQX	Wire, Guide, Catheter	Cardiovascular	Class 2	870.1330	2010-10-21

Official Correspondent

Rich Brown

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Confluent Medical Technologies, 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
3013668043	CONFLUENT MEDICAL TECHNOLOGIES, INC.	Warwick, RI, US
3009018440	Nitinol Devices & Components Costa Rica, S. R. L.	El Coyol Alajuela, CR

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K150445	Asahi Intecc Co., Ltd.	ASAHI Peripheral Guide Wire Series (ASAHI Gladius, ASAHI Halberd, ASAHI Gaia PV)	2015-06-30
K082922	Lake Region Mfg., Inc.	FREEWAY AND RAILRUNNER GUIDEWIRES	2008-12-09
K890207	E-Z-Em, Inc.	INTERVENTIONAL PRODUCTS - GUIDE WIRES	1989-05-31
K992169	Advanced Cardiovascular Systems, Inc.	ACS HI-TORQUE CROSS-IT 400XT GUIDE WIRE	1999-10-28
K012534	Advanced Cardiovascular Systems, Inc.	HI-TORQUE MIDDLE SUPPORT .012 GUIDE WIRE WITH HYDROCOAT HYDROPHILIC COATING	2002-01-24

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0030-2009	Boston Scientific Corporation	2	Platinum Plus" LT , REF 46-601, UPN M001466010, LT/0.018/180, Sterilized with ethylene oxide gas, Rx only, Legal Manufacturer Boston Scientific Corporation, One Boston scientific Place, Natick, MA 01760-1537, Made in USA: 8600 NW 41st Street, Miami, FL 33166-6202. The Platinum Plus" Guidewire facilitates placement of a catheter during diagnostic or interventional intravascular procedures. The wire can be torqued to facilitate navigation through tortuous arteries and/or avoid unwanted side branches.
Z-0031-2009	Boston Scientific Corporation	2	Platinum Plus" LT , REF 46-602, UPN M001466020, LT/0.018/260, Sterilized with ethylene oxide gas, Rx only, Legal Manufacturer Boston Scientific Corporation, One Boston scientific Place, Natick, MA 01760-1537, Made in USA: 8600 NW 41st Street, Miami, FL 33166-6202. The Platinum Plus" Guidewire facilitates placement of a catheter during diagnostic or interventional intravascular procedures. The wire can be torqued to facilitate navigation through tortuous arteries and/or avoid unwanted side branches.

Similar Registrations

Registration Number	Establishment Name	Location
3024743081	EMBRACE MEDICAL LTD.	Tel Aviv, IL
3042175841	PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.	Best Noord-Brabant, NL
3018070217	SHANGHAI ACHIEVA MEDICAL SUZHOU CO., LTD.	Suzhou Jiangsu, CN
3015522130	NANO4IMAGING USA, LLC.	Dublin, OH, US
1225687	Boston Scientific Corp., Marina Bay Cust. Fulfillment Center	QUINCY, MA, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3007635982. Last updated year: 2026. Please use registration number 3007635982 when referencing this establishment in official correspondence.