FDA Device Intelligence
Home › Hebei Zhemai Technology Co., Ltd. › ZHEONE

ZHEONE

Hebei Zhemai Technology Co., Ltd. · Model FI-L06 · UDI-DI 06977620360019

ONF
1
510(k) clearances
32
Adverse events
0
Recalls
98
Facilities

Description

The Intense pulsed light therapy device is indicated for use in surgical and aesthetic applications in permanent hair removal. Permanent hair reduction is defined as the long-term, stable reduction in the number of hairs regrowing when measured at 6, 9, and 12 months after the completion of a treatment regimen.

Query this across every FDA database — by API.

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

Get your free API keyRead the docs
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.