Class Class II

NEW DOUBLO 2.0 (K251334)

K251334 2025-09-29 Traditional
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Description

NEW DOUBLO 2.0 by Hironic Co., Ltd., an FDA 510(k) cleared general, plastic surgery device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK251334
Clearance Date2025-09-29
Clearance TypeTraditional
Product CodeGEI
Regulation Number878.4400

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