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Recognized a 510(k)/PMA number — showing its clearance record and devices.

Clearance record K251973

Luminance Red Cold Sore Device (TN1927G) · Luminance Medical Ventures, Inc. · decided 2025-09-23 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
Luminance RED Cold Sore DeviceTN1927GLuminance Medical Ventures IncorporatedOKJ00850063220064