Data / Medical devices / United States / Valencia Technologies Corporation

Valencia Technologies Corporation: FDA-registered device maker in Valencia, CA, United States, 1 PMA approval

Name: Valencia Technologies Corporation FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

Valencia Technologies Corporation is registered with the FDA (registration 3010878085) in Valencia, CA, United States. It lists 4 device types. The FDA files 1 PMA approval under its listings, the newest dated March 1, 2022. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number: 3010878085
Address: 28464 Westinghouse Place, Valencia, CA, United States, 91355
Owner or operator: Boston Scientific Corporation (9912058)
Roles: Complaint file establishment, Manufacturer, Specification developer
First device listed: May 1, 2026
Registered through: 2026
Brand names listed: eCoin Device Kit, eCoin External Controller Kit, eCoin Patient Kit

Devices it lists

Device	Product code	Class	Role	Source
Dressing Change Tray	OXQ	1	Complaint file establishment, Manufacturer, Specification developer	accessdata.fda.gov
General Surgery Tray	LRO	2	Complaint file establishment, Manufacturer, Specification developer	accessdata.fda.gov
Instrument, Surgical, Non-Powered	HAO	1	Complaint file establishment, Manufacturer, Specification developer	accessdata.fda.gov
Stimulator, Tibial, Electrical, Implantable, For Urinary Incontinence	QPT	3	Complaint file establishment, Manufacturer, Specification developer	accessdata.fda.gov

PMA approvals

Premarket approvals this establishment lists, with the supplements the FDA has decided since.

Approved	PMA number	Device	Product code	Supplements	Latest decision	Source
March 1, 2022	P200036	eCoin Peripheral Neurostimulator	QPT	10	September 9, 2026	accessdata.fda.gov

Compare with other makers

Updated September 9, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.