Class Class II

InbellaIgnite RF System (K251435)

K251435 2026-01-27 Traditional
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Description

InbellaIgnite RF System by Inbella Medical, Inc., an FDA 510(k) cleared general, plastic surgery device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK251435
Clearance Date2026-01-27
Clearance TypeTraditional
Product CodeGEI
Regulation Number878.4400

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