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Data / Medical devices / Belarus / Solar LS CJSC

Solar LS CJSC: FDA-registered device maker in Minsk, Belarus, 1 510(k) clearance

Solar LS CJSC is registered with the FDA (registration 3045892905) in Minsk, Belarus. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated March 21, 2025. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3045892905
Address
4 Stebeneva lane, Minsk, Belarus, 220024
Owner or operator
SOLAR LS CJSC (10095863)
Roles
Manufacturer
First device listed
May 12, 2026
Registered through
2026
Brand names listed
Evoline, Evoline Platinum, Medical Laser System Incanto

Devices it lists

DeviceProduct codeClassRoleSource
Powered Laser Surgical InstrumentGEX2Manufactureraccessdata.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
March 21, 2025K243630Medical Laser System Incanto / Evoline Platinum /EvolineGEXSubstantially EquivalentSolar LS Cjscaccessdata.fda.gov

Compare with other makers

Updated March 21, 2025. 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.