Acotec Scientific Co., Ltd.

Acotec Scientific Co., Ltd. holds 1 FDA 510(k) medical device clearance, cleared in 2025.

Top product codes for Acotec Scientific Co., Ltd.

GEI — General, Plastic Surgery1 device

Recent clearances by Acotec Scientific Co., Ltd.

K250688 — Cedar Endovenous Radiofrequency Catheter (ERA-C70-US) +2 moreCode GEI·2025-10-07

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