Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3016540856

FEI Number

3016540856

Entity Name

NeuroVasc Technologies, Inc.

City/State/Country

Irvine, CA, US

Establishment Address

3 Jenner, Ste 100, Irvine, CA 92618, US

Establishment Type(s)

Manufacture Device in the United States for Export Only

Owner / Operator

NeuroVasc Technologies, Inc. (Owner Number: 10056393)

Owner / Operator Contact Address

3 Jenner, Suite 100, Irvine, CA 92618, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Envion Detachable Coils

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HCG	Device, Neurovascular Embolization	Neurology	Class 2	882.5950	2026-04-16

Official Correspondent

Edgar Trejo Gimenez

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

NeuroVasc Technologies, Inc.

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

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K951256	Target Therapeutics	DETACHABLE PLATINUM COIL (GUGLIELMI DETACHABLE COIL, GDC)	1995-09-08

Similar Registrations

Registration Number	Establishment Name	Location
9615728	BIOSPHERE MEDICAL, S.A.	Roissy Val-d'Oise, FR
2029275	Sterigenics U.S., LLC	Corona, CA, US
3008853977	Stryker Neurovascular	Fremont, CA, US
2022435	Sterigenics U.S., LLC	Tustin, CA, US
1721676	Sterigenics U.S., LLC	Salt Lake City, UT, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3016540856. Last updated year: 2026. Please use registration number 3016540856 when referencing this establishment in official correspondence.