Acotec Scientific Co., Ltd.

1FDA 510(k) medical device clearance.

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); Cedar Endovenous Radiofrequency Catheter (ERA-C30-US); Endovenous Radiofrequency Generator (ERA-G5-US)Code GEI·2025-10-07

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