FDA Device Intelligence
Home › Shenzhen Bosidin Technology Co.,Ltd. › Bosidin

Bosidin

Shenzhen Bosidin Technology Co.,Ltd. · Model D-1129 · UDI-DI 06970112301293

OHT
1
510(k) clearances
32
Adverse events (1 deaths)
0
Recalls
92
Facilities

Description

The Device is an over-the-counter device intended for removal of unwanted body and/or facial hair.

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.