Class Class II

Legend X Platform (K252576)

K252576 2025-09-12 Special
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Description

Legend X Platform by Pollogen, Ltd., an FDA 510(k) cleared general, plastic surgery device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK252576
Clearance Date2025-09-12
Clearance TypeSpecial
Product CodeGEI
Regulation Number878.4400

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