Companies / Multi Radiance Medical

Medical device company profile

Multi Radiance Medical

Super-pulsed therapeutic laser systems for non-invasive pain-management applications.

Medical Device ManufacturerNeurology, Mental Health & PainOrthopedics & MusculoskeletalPain ManagementRehabilitation & RecoveryCommercial-stage

Headquarters🇺🇸Solon, Ohio, United States

FoundedNot confirmed

Commercial statusCommercially availableSelected products commercially offered; availability and indications vary by product and market.

EmployeesNot confirmed

Estimated revenueNot confirmed

Official websitewww.multiradiance.com ↗

Company overview

Multi Radiance Medical develops therapeutic light and laser systems for pain-management practices. Its portfolio combines super-pulsed laser and other light sources in devices intended for labeled temporary symptom relief, with separate human and veterinary offerings.

FibroLux is a distinct human-use therapeutic laser with a reviewed FDA clearance for adjunctive relief of pain associated with fibromyalgia. The profile ties that authorization to the named device and indication rather than treating all laser models or treatment protocols as interchangeable.

The company operates from Solon, Ohio, and identifies Max Kanarsky as President and CEO in its official FibroLux announcement. Commercial delivery includes clinician education and distribution relationships. Broader pain indications and newer announcements require model-specific review before being added to the regulatory snapshot.

^{[13][14][15][16][17]}

Leadership

1 people

Max KanarskyPresident & Chief Executive Officer ^[17]

Products & regulatory status How does MedTechIndex get this information?

Summary

Multi Radiance’s human-use laser portfolio includes FibroLux’s fibromyalgia-related clearance and later MR5 Activ Pro decision K254024. FDA records also document earlier MR4/TerraQuant lineage. Human and veterinary products, and U.S. versus overseas indications, must be kept distinct. ^{[13][17][12][6][16][15][1]}

No matching FDA recall event was identified in the completed company/applicant, linked-identifier and product-name searches. ^[10][8]

Regulatory snapshot How to read this snapshot

U.S. FDA

5
510(k) clearances: 0
De Novo grants: 0
PMA approvals: 0
Recall events

Latest recorded source review: 2026-10-20.

Commercial portfolio snapshot

Documented commercial product families.

Therapeutic laser

FibroLux ↗

Non-invasive therapeutic laser with device-specific FDA clearance. ^[13][12]

FDA-cleared

Commercially offered; exact model and country availability should be confirmed with the manufacturer.

Therapeutic light / laser systems

Human pain-management laser portfolio ↗

Commercial laser systems and accessories; model-specific indications are not comprehensively mapped. ^[13]

Marketed · regulatory scope varies

Commercially offered; exact model and country availability should be confirmed with the manufacturer.

Commercial development

Commercial human-use therapeutic lasers; selected FibroLux indication separated from other models, veterinary devices and unreviewed expanded claims. ^[13][17][12]

Activity & Milestones

1 events

2022-09-02 · Regulatory

FibroLux cleared

FDA documented K212189 for the FibroLux device. ^[12]

17 Cited Sources

Accessed 10/20/2026

[1] FDA 510(k) database — research search ↗FDA / openFDA · regulatory record

[2] FDA K061614 — TERRAQUANT MQ2000 V. 5 AND HANDYRX MQ2007 LASERS ↗U.S. Food and Drug Administration · regulatory record

[3] FDA K080102 — TQ SOLO AND SOLO PRO AND LS50 ACCESSORY AND MR4 MULTI RADIANCE THERAPY SYSTEM ↗U.S. Food and Drug Administration · regulatory record

[4] FDA K171354 — MR4 Laser ↗U.S. Food and Drug Administration · regulatory record

[5] FDA K212189 — FibroLux ↗U.S. Food and Drug Administration · regulatory record

[6] FDA K254024 — MR5 Activ Pro ↗U.S. Food and Drug Administration · regulatory record

[7] FDA De Novo database — research search ↗FDA / openFDA · regulatory record

[8] FDA medical-device recall database — research search ↗FDA / openFDA · regulatory record

[9] FDA PMA database — research search ↗FDA / openFDA · regulatory record

[10] FDA medical-device recall database — research search ↗FDA / openFDA · regulatory record

[11] FDA UDI database — research search ↗FDA / openFDA · regulatory record

[12] FDA 510(k) K212189 ↗U.S. Food and Drug Administration · regulatory database

[13] Human therapeutic laser portfolio ↗Multi Radiance Medical · company website

[14] Company and clinical technology overview ↗Multi Radiance Medical · company website

[15] Employer hiring source reviewed ↗Multi Radiance Medical · company website

[16] Official press-release archive ↗Multi Radiance Medical · company website

[17] FibroLux clearance and company leadership ↗Multi Radiance Medical · company website