Class Class II

Diode laser therapy device (VADER) (K251457)

K251457 2025-09-03 Traditional
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Description

Diode laser therapy device (VADER) by Beijing Superlaser Technology Co., Ltd., an FDA 510(k) cleared general, plastic surgery device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK251457
Clearance Date2025-09-03
Clearance TypeTraditional
Product CodeGEX
Regulation Number878.4810

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