Class Class II

CuRAS hybrid (K253123)

K253123 2025-11-20 Traditional
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Description

CuRAS hybrid by Classys, Inc., an FDA 510(k) cleared general, plastic surgery device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK253123
Clearance Date2025-11-20
Clearance TypeTraditional
Product CodeGEX
Regulation Number878.4810

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