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Lamidey Noury Medical: FDA-registered device maker in Verrieres Le Buisson Essonne, France, 2 510(k) clearances

Name: Lamidey Noury Medical FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

Lamidey Noury Medical is registered with the FDA (registration 3015286855) in Verrieres Le Buisson Essonne, France. It lists 4 device types. The FDA files 2 510(k) clearances under its listings, the newest dated June 12, 2024. Registered through 2026. FDA data exported November 3, 2026.

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FDA registration number: 3015286855
Address: 3 rue des petits ruisseaux, Verrieres Le Buisson Essonne, France, 91370
Owner or operator: Lamidey Noury Medical (10084684)
Roles: Manufacturer
First device listed: November 23, 2022
Registered through: 2026
Brand names listed: PLASMA EDGE

Devices it lists

Device	Product code	Class	Role	Source
Electrode, Electrosurgical, Active, Urological	FAS	2	Manufacturer	accessdata.fda.gov
Electrosurgical, Cutting & Coagulation & Accessories	GEI	2	Manufacturer	accessdata.fda.gov
Resectoscope, Working Element	FDC	2	Manufacturer	accessdata.fda.gov
Unit, Electrosurgical, Endoscopic (With Or Without Accessories)	KNS	2	Manufacturer	accessdata.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.

Decided	510(k) number	Device	Product code	Decision	Applicant	Source
June 12, 2024	K240504	PLASMA EDGE System	FAS	Substantially Equivalent	Lamidey Noury Medical	accessdata.fda.gov
September 21, 2022	K222542	MCB UNIT Model: V10GMCBUS	KNS	Substantially Equivalent	Lamidey Noury Medical	accessdata.fda.gov

Compare with other makers

Updated June 12, 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.