Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

2435300

FEI Number

2435300

Entity Name

VASOMEDICAL, INC.

City/State/Country

Plainview, NY, US

Establishment Address

137 Commercial St Ste 200, Plainview, NY 11803, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

VASOMEDICAL, INC. (Owner Number: 2435300)

Owner / Operator Contact Address

137 Commercial St., Unit 200, Plainview, NY 11803, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K033617

PMA Number

N/A

All Registered Proprietary Names

EECP Lumenair AngioNew Enhanced External Counterpulsation

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
DRN	Device, Counter-Pulsating, External	Cardiovascular	Class 2	870.5225	2007-12-05

Official Correspondent

Matthew McClure

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

VASOMEDICAL, 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
3007663004	Biox Instruments Co Ltd	Wuxi Jiangsu, CN

Similar Registrations

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3002806999	VAMED MEDICAL INSTRUMENT CO.,LTD	Foshan Guangdong, CN
3012470925	XTREEM PULSE	New York, NY, US
3010564728	RENEW GROUP PRIVATE LIMITED	Singapore Central Singapore, SG

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2435300. Last updated year: 2026. Please use registration number 2435300 when referencing this establishment in official correspondence.