Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3011693567

FEI Number

3011693567

Entity Name

LAMINATE MEDICAL TECHNOLOGIES

City/State/Country

Tel Aviv, IL

Establishment Address

24 Raoul Wallenberg St, Tel Aviv 6971921, IL

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Laminate Medical Technologies (Owner Number: 10057803)

Owner / Operator Contact Address

24 Raoul Wallenberg St, Tel Aviv, IL-TA 6971921, IL

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

VasQ VasQ DMST - Disposable Model Selection Tool

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
QVQ	Extravascular Support For An Arteriovenous Fistula For Vascular Access	Cardiovascular	Class 2	870.4600	2024-02-18
QVQ	Extravascular Support For An Arteriovenous Fistula For Vascular Access	Cardiovascular	Class 2	870.4600	2023-10-05
FTY	Tape, Measuring, Rulers And Calipers	General, Plastic Surgery	Class 1	878.4800	2018-05-29

Official Correspondent

Orit Yarden

US Agent Details

Anthony Rodriguez Business: Laminate Medical Technologies Email: anthony@laminatemedical.com Phone: (512) 6730891

Related Public Records

Same Entity

Laminate Medical Technologies

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 3011693567. Last updated year: 2026. Please use registration number 3011693567 when referencing this establishment in official correspondence.