Skip to the page

Data / Medical devices / Israel / Laminate Medical Technologies

Laminate Medical Technologies: FDA-registered device maker in Tel Aviv, Israel, 2 510(k) clearances

Laminate Medical Technologies is registered with the FDA (registration 3011693567) in Tel Aviv, Israel. It lists 2 device types. The FDA files 2 510(k) clearances under its listings, the newest dated February 16, 2024. Registered through 2026. FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

FDA registration number
3011693567
Address
24 Raoul Wallenberg St, Tel Aviv, Israel, 6971921
Owner or operator
Laminate Medical Technologies (10057803)
Roles
Manufacturer
First device listed
May 29, 2018
Registered through
2026
Brand names listed
DMST - Disposable Model Selection Tool, VasQ

Devices it lists

DeviceProduct codeClassRoleSource
Extravascular Support For An Arteriovenous Fistula For Vascular AccessQVQ2Manufactureraccessdata.fda.gov
Tape, Measuring, Rulers And CalipersFTY1Manufactureraccessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
February 16, 2024K240119VasQQVQSubstantially EquivalentLaminate Medical Technologies , Ltd.accessdata.fda.gov
September 26, 2023DEN220026VasQQVQUnknownLaminate Medical Technologies , Ltd.accessdata.fda.gov

Compare with other makers

Updated February 16, 2024. 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.