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Vellus

Shenzhen Leaflife Technology Co., Ltd. · Model HYPER HR · UDI-DI 06974223650103

OHT Prescription
1
510(k) clearances
35
Adverse events (1 deaths)
0
Recalls
93
Facilities

Description

Vellus LED Therapy device

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.