Class Class II

WinForth (LM-E470KA) (K250916)

K250916 2025-08-14 Traditional
Home/ Devices/ WinForth (LM-E470KA) (K250916)

Description

WinForth (LM-E470KA) by Shenzhen Leaflife Technology Co., Ltd., an FDA 510(k) cleared general, plastic surgery device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK250916
Clearance Date2025-08-14
Clearance TypeTraditional
Product CodePBX
Regulation Number878.4400

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