Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3010878085

FEI Number

3010878085

Entity Name

VALENCIA TECHNOLOGIES CORPORATION

City/State/Country

Valencia, CA, US

Establishment Address

28464 Westinghouse Place, Valencia, CA 91355, US

Establishment Type(s)

Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device,Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

Boston Scientific Corporation (Owner Number: 9912058)

Owner / Operator Contact Address

300 Boston Scientific Way, Marlborough, MA 01752, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

eCoin Patient Kit eCoin External Controller Kit eCoin Device Kit

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HAO	Instrument, Surgical, Non-Powered	Neurology	Class 1	882.4535	2026-05-01
LRO	General Surgery Tray	General, Plastic Surgery	Class 2	878.4370	2026-05-01
QPT	Stimulator, Tibial, Electrical, Implantable, For Urinary Incontinence	Unknown	Class 3	N/A	2026-05-01
OXQ	Dressing Change Tray	General Hospital	Class 1	880.5075	2026-05-01

Official Correspondent

Adrienne Bishop

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Boston Scientific Corporation

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

View Entity Profile →

Other Registrations for Same Entity

Registration Number	Establishment Name	Location
3025434462	Obsidio Inc	Maple Grove, MN, US
3005619880	Boston Scientific Corporation	Roswell, GA, US
3015425075	NALU MEDICAL	Carlsbad, CA, US
3015289131	FARAPULSE, INC.	Menlo Park, CA, US
3022298579	Boston Scientific Cardiac Diagnostic Technologies, Inc.	Arden Hills, MN, US

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K961683	J.J. Skinner, Inc.	JJ SKINNER CAREKITS MINOR SURGICAL PROCEDURE TRAY	1996-05-10

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0009-2024	Boston Scientific Corporation	2	Guider Softip Guide Catheter 6F PRE-SHAPED 40 90CM, Catalog number H965100420, cardiac guide catheter
Z-0010-2024	Boston Scientific Corporation	2	Guider Softip Guide Catheter 7F PRE-SHAPED 40 90CM, Catalog number H965100430, cardiac guide catheter
Z-0011-2024	Boston Scientific Corporation	2	Guider Softip Guide Catheter 8F PRE-SHAPED 40 90CM, Catalog number H965100440, cardiac guide catheter
Z-0012-2024	Boston Scientific Corporation	2	Guider Softip Guide Catheter 6F 90CM MULTI PURPOSE, Catalog number H965100460, cardiac guide catheter
Z-0013-2024	Boston Scientific Corporation	2	Guider Softip Guide Catheter 7F 90CM MULTI PURPOSE, Catalog number H965100470, cardiac guide catheter

Similar Registrations

Registration Number	Establishment Name	Location
3026820968	NEURGAIN TECHNOLOGIES	La Jolla, CA, US
3006247277	OPTICO LTD	LETCHWORTH Hertfordshire, GB
3005621335	DEVEMED GMBH	NEUHAUSEN OB ECK Baden-Wurttemberg, DE
2126670	SCANLAN INTERNATIONAL, INC.	Saint Paul, MN, US
3012833053	PATHWAY MEDTECH, LLC.	Santee, CA, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010878085. Last updated year: 2026. Please use registration number 3010878085 when referencing this establishment in official correspondence.