Class Class II

MEDILIGHT (K231952)

K231952 2025-09-03 Special
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Description

MEDILIGHT by Medicreations, LLC, an FDA 510(k) cleared general, plastic surgery device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK231952
Clearance Date2025-09-03
Clearance TypeSpecial
Product CodeONF
Regulation Number878.4810

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