Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3034300126

FEI Number

3034300126

Entity Name

NOVA VASCULAR LLC

City/State/Country

New York, NY, US

Establishment Address

99 Wall St # 878, New York, NY 10005, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

Nova Vascular LLC (Owner Number: 10093640)

Owner / Operator Contact Address

99 Wall St. 878, New York, NY 10005, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Nova Vascular Multi-Stage Balloon Catheter

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
GBA	Catheter, Balloon Type	General, Plastic Surgery	Class 1	878.4200	2025-06-16

Official Correspondent

Alon Bolotin

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Nova Vascular LLC

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

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3034300126. Last updated year: 2026. Please use registration number 3034300126 when referencing this establishment in official correspondence.