Bomtech Electronics Co., Ltd.

Bomtech Electronics Co., Ltd. holds 2 FDA 510(k) medical device clearances, first cleared 2024, most recent 2025.

Top product codes for Bomtech Electronics Co., Ltd.

GEI — General, Plastic Surgery1 device
QAI — General, Plastic Surgery1 device

Recent clearances by Bomtech Electronics Co., Ltd.

K243143 — E-PEN (E-PEN)Code QAI·2025-04-07
K243097 — RM STAR EX with RMS NeedleCode GEI·2024-12-26

Data sourced from openFDA. This site is unofficial and independent of the FDA.