Ceramoptec GmbH

Ceramoptec GmbH holds 2 FDA 510(k) medical device clearances, first cleared 2021, most recent 2025.

Top product codes for Ceramoptec GmbH

GEX — General, Plastic Surgery2 devices

Recent clearances by Ceramoptec GmbH

K250504 — Leonardo DusterCode GEX·2025-07-14
K210951 — Leonardo Mini BlueCode GEX·2021-09-01

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