Data / Medical devices / United States / Medical Quant Usa

Medical Quant Usa: FDA-registered device maker in Solon, OH, United States, 7 510(k) clearances

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

Medical Quant Usa is registered with the FDA (registration 3005730446) in Solon, OH, United States. It lists 6 device types. The FDA files 7 510(k) clearances under its listings, the newest dated June 10, 2026. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number: 3005730446
Address: 6521 Davis Industrial Pkwy, Solon, OH, United States, 44139
Owner or operator: Multi Radiance Medical (9087202)
Roles: Manufacturer, Repackager or relabeler, Specification developer
First device listed: June 1, 2012
Registered through: 2026
Brand names listed: Contoura Laser Stim, Fibrolux, Force-X CX5, Force-X CX7, HOLISTIC BODY SHOP RELIEF+, LS50 Emitter, Laser STIM Target Emitter, Laser Shower LS50 and more

Devices it lists

Device	Product code	Class	Role	Source
Lamp, Infrared, Therapeutic Heating	ILY	2	Manufacturer, Repackager or relabeler	accessdata.fda.gov
Massager, Powered Inflatable Tube	IRP	2	Specification developer	accessdata.fda.gov
Pack, Hot Or Cold, Water Circulating	ILO	2	Specification developer	accessdata.fda.gov
Powered Laser Surgical Instrument	GEX	2	Manufacturer, Repackager or relabeler	accessdata.fda.gov
Powered Light Based Laser Non-Thermal Instrument With Non-Heating Effect For Adjunctive Use In Pain Therapy	NHN	2	Manufacturer, Repackager or relabeler	accessdata.fda.gov
Stimulator, Nerve, Transcutaneous, For Pain Relief	GZJ	2	Manufacturer, Repackager or relabeler	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 10, 2026	K253919	Cryo And Thermo Therapy System	IRP	Substantially Equivalent	Xiamen Weiyou Intelligent Technology Co., Ltd.	accessdata.fda.gov
May 19, 2026	K254024	MR5 Activ Pro	NHN	Substantially Equivalent	Multi Radiance Medical, Inc.	accessdata.fda.gov
September 2, 2022	K212189	FibroLux	NHN	Substantially Equivalent	Multi Radiance Medical	accessdata.fda.gov
January 13, 2018	K171354	MR4 Laser	NHN	Substantially Equivalent	Multi Radiance Medical	accessdata.fda.gov
August 20, 2008	K080102	TQ SOLO AND SOLO PRO AND LS50 ACCESSORY AND MR4 MULTI RADIANCE THERAPY SYSTEM	ILY	Substantially Equivalent	Escada International, Inc.	accessdata.fda.gov
October 29, 2007	K071445	TERRAQUANT MQ2000 V.5 WITH THE TQ-1TENS	ILY	Substantially Equivalent	Escada International, Inc.	accessdata.fda.gov
October 6, 2006	K061614	TERRAQUANT MQ2000 V. 5 AND HANDYRX MQ2007 LASERS	ILY	Substantially Equivalent	Escada International, Inc.	accessdata.fda.gov

Compare with other makers

Updated June 10, 2026. 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.