Class Class II

LED Light Therapy Device (Models: SG-FM, SG-FE) (K253086)

K253086 2025-12-19 Traditional
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Description

LED Light Therapy Device (Models: SG-FM, SG-FE) by Sunglor Technology Co., Ltd., an FDA 510(k) cleared general, plastic surgery device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK253086
Clearance Date2025-12-19
Clearance TypeTraditional
Product CodeOHS
Regulation Number878.4810

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