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

Clearance record K232153

Avéli · Revelle Aesthetics, Inc. · decided 2023-08-18 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
AveliAVE002Revelle Aesthetics, Inc.FTD GDI OUP00850036790013
AveliAVE001Revelle Aesthetics, Inc.FTD GDI OUP00850036790006